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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_001002258.5 → NP_001002258.1 ATP synthase F(0) complex subunit C3, mitochondrial isoform A precursor
See identical proteins and their annotated locations for NP_001002258.1
Status: REVIEWED
- Description
- Transcript Variant: This variant (3) has multiple differences in the presence and absence of intron sequences at the 5' and 3' ends, compared to variant 4. These differences result in a protein (isoform A) with a longer C-terminus, compared to isoform B. Variants 2 and 3 encode the same protein.
- Source sequence(s)
-
AC096649, AW025164, U09813
- Consensus CDS
-
CCDS2263.1
- UniProtKB/Swiss-Prot
- B2R4Z0, D3DPF0, P48201, Q4ZFX7
- UniProtKB/TrEMBL
-
Q6LEU9
- Related
- ENSP00000376324.3, ENST00000392541.3
- Conserved Domains (1) summary
-
- MTH00222
Location:68 → 142
- ATP9; ATP synthase F0 subunit 9; Provisional
-
NM_001190329.2 → NP_001177258.1 ATP synthase F(0) complex subunit C3, mitochondrial isoform B precursor
See identical proteins and their annotated locations for NP_001177258.1
Status: REVIEWED
- Description
- Transcript Variant: This variant (4) represents the longest transcript but encodes a shorter protein (isoform B), compared to isoform A. Isoform B is predicted to lack a complete ATP synthase subunit C domain.
- Source sequence(s)
-
AC096649, AW025164, BF210704, BI765737
- Conserved Domains (1) summary
-
- cl00466
Location:68 → 105
- ATP-synt_C; ATP synthase subunit C
-
NM_001689.5 → NP_001680.1 ATP synthase F(0) complex subunit C3, mitochondrial isoform A precursor
See identical proteins and their annotated locations for NP_001680.1
Status: REVIEWED
- Description
- Transcript Variant: This variant (2) has an additional intron sequence in its 3' end, compared to variant 4. This difference results in a protein (isoform A) with a longer C-terminus, compared to isoform B. Variants 2 and 3 encode the same protein.
- Source sequence(s)
-
AC096649, AW025164, BC106881, BF210704, BI756002
- Consensus CDS
-
CCDS2263.1
- UniProtKB/Swiss-Prot
- B2R4Z0, D3DPF0, P48201, Q4ZFX7
- UniProtKB/TrEMBL
-
Q6LEU9
- Related
- ENSP00000284727.4, ENST00000284727.9
- Conserved Domains (1) summary
-
- MTH00222
Location:68 → 142
- ATP9; ATP synthase F0 subunit 9; Provisional
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 GRCh38.p14 Primary Assembly
Genomic
-
NC_000002.12 Reference GRCh38.p14 Primary Assembly
- Range
-
175176258..175181710 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
Alternate T2T-CHM13v2.0
Genomic
-
NC_060926.1 Alternate T2T-CHM13v2.0
- Range
-
175665044..175670493 complement
- 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_001002256.1: Suppressed sequence
- Description
- NM_001002256.1: This RefSeq record was removed by NCBI staff. Contact info@ncbi.nlm.nih.gov for further information.