ClinVar

NM_001127222.2(CACNA1A):c.3227C>T (p.Ala1076Val)

Gene:

CACNA1A:calcium voltage-gated channel subunit alpha1 A [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

19p13.13

Genomic location:

• Chr19: 13286829 (on Assembly GRCh38)
• Chr19: 13397643 (on Assembly GRCh37)

Preferred name:

NM_001127222.2(CACNA1A):c.3227C>T (p.Ala1076Val)

HGVS:

• NC_000019.10:g.13286829G>A
• NG_011569.1:g.224632C>T
• NM_000068.4:c.3239C>T
• NM_001127221.2:c.3230C>T
• NM_001127222.2:c.3227C>TMANE SELECT
• NM_001174080.2:c.3230C>T
• NM_023035.3:c.3239C>T
• NP_000059.3:p.Ala1080Val
• NP_001120693.1:p.Ala1077Val
• NP_001120693.1:p.Ala1077Val
• NP_001120694.1:p.Ala1076Val
• NP_001167551.1:p.Ala1077Val
• NP_075461.2:p.Ala1080Val
• LRG_7t1:c.3230C>T
• LRG_7:g.224632C>T
• LRG_7p1:p.Ala1077Val
• NC_000019.9:g.13397643G>A
• NM_000068.2:c.3230C>T
• NM_001127221.1:c.3230C>T
• NM_023035.2:c.3239C>T

This HGVS expression did not pass validation

Protein change:

A1076V

Links:

dbSNP: rs199512932

NCBI 1000 Genomes Browser:

rs199512932

Molecular consequence:

• NM_000068.4:c.3239C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001127221.2:c.3230C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001127222.2:c.3227C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001174080.2:c.3230C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_023035.3:c.3239C>T - missense variant - [Sequence Ontology: SO:0001583]

Observations:

1