These reference sequences exist independently of genome builds. Explain
These reference sequences are curated independently of the genome
annotation cycle, so their versions may not match the RefSeq versions in the current
genome build. Identify version mismatches by comparing the version of the RefSeq in this
section to the one reported in Genomic regions, transcripts, and products above.
mRNA and Protein(s)
-
NM_001008405.2 → NP_001008405.1 B-cell receptor-associated protein 29 isoform a
Status: VALIDATED
- Description
- Transcript Variant: This variant (1) represents the shortest transcript but encodes the longer isoform (a).
- Source sequence(s)
-
AI684765, AK000878, AK289401, AW994087, BE006248, BF434482, BM931263, BP261060, BX101190, BX647653, DA569360, EB388415, H40966
- Consensus CDS
-
CCDS34730.1
- UniProtKB/TrEMBL
-
E9PAJ1
- UniProtKB/TrEMBL
-
G5E9L4
- Related
- ENSP00000368414, ENST00000379119
- Conserved Domains (1) summary
-
- cl02219
Location:1 – 220
Blast Score: 425
- Bap31; B-cell receptor-associated protein 31-like
-
NM_018844.3 → NP_061332.2 B-cell receptor-associated protein 29 isoform b
Status: VALIDATED
- Description
- Transcript Variant: This variant (2) differs in the 5' UTR, and lacks an alternate exon in the 3' coding region that causes a frameshift, compared to variant 1. The resulting isoform (b) is shorter and has a distinct C-terminus, compared to isoform a.
- Source sequence(s)
-
AI684765, AK000878, AK289401, AW994087, BE006248, BF434482, BG776708, BM931263, BX101190, BX647653, DA569360, DA717500, EB388415, H40966
- Consensus CDS
-
CCDS34731.1
- UniProtKB/TrEMBL
-
E9PAJ1
- UniProtKB/Swiss-Prot
-
Q9UHQ4
- Related
- ENSP00000005259, OTTHUMP00000206633, ENST00000005259, OTTHUMT00000337011
- Conserved Domains (1) summary
-
- cl02219
Location:1 – 220
Blast Score: 423
- Bap31; B-cell receptor-associated protein 31-like
RNA
-
NR_027830.1 RNA Sequence
- Description
- Transcript Variant: This variant (3) differs in the 5' region and lacks an exon in the 3' region, compared to variant 1. This variant is represented as non-coding because it lacks a portion of the 5' coding region including the translational start codon, compared to variant 1, and there is uncertainty about its coding capacity.
- Source sequence(s)
-
AI684765, AK000878, AK294824, AW994087, BE006248, BF434482, BG776708, BM931263, BX101190, BX647653, DA569360, DA717500, EB388415, H40966
The following sections contain reference sequences that belong to a
specific genome build. Explain
This section includes genomic Reference
Sequences (RefSeqs) from all assemblies on which this gene is annotated, such as RefSeqs
for chromosomes and scaffolds (contigs) from both reference and alternate assemblies.
Model RNAs and proteins are also reported here.
Reference GRCh37.p5 Primary Assembly
Genomic
-
NC_000007.13 Reference GRCh37.p5 Primary Assembly
- Range
- 107220422..107263762
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
Alternate HuRef
Genomic
-
AC_000139.1 Alternate HuRef
- Range
- 101581486..101624158
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
Alternate CRA_TCAGchr7v2
Genomic
-
AC_000068.1 Alternate CRA_TCAGchr7v2
- Range
- 106581511..106624867
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
The following Reference Sequences have been suppressed. Explain
These RefSeqs were suppressed for the cited
reason(s). Suppressed RefSeqs do not appear in BLAST databases, related sequence links,
or BLAST links (BLink), but may still be retrieved by clicking on their
accession.version below.
-
NM_001008406.1: Suppressed sequence
- Description
- NM_001008406.1: This RefSeq was permanently suppressed because currently there is insufficient support for the transcript and the protein.
-
NM_001008407.1: Suppressed sequence
- Description
- NM_001008407.1: This RefSeq was permanently suppressed because currently there is insufficient support for the transcript and the protein.