Canonical Allele Identifier: CA422689061
Gene: CACNA1S HGNC NCBI

Linked Data

ClinVar Variation Id: 3072603
ClinVar RCV Id: RCV004013625
MyVariant Identifiers: chr1:g.201044702C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201075574C>T , CM000663.2:g.201075574C>T GRCh38
NC_000001.10:g.201044702C>T , CM000663.1:g.201044702C>T GRCh37
NC_000001.9:g.199311325C>T NCBI36
NG_009816.1:g.41993G>A
NG_009816.2:g.41993G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000362061.4:c.1869G>A MANE Select ENSP00000355192.3:p.Gly623=
ENST00000679417.1:c.*1032G>A ENSP00000506706.1:n.*1032G>A
ENST00000680059.1:c.1869G>A ENSP00000504944.1:p.Gly623=
ENST00000681078.1:c.1869G>A ENSP00000506645.1:p.Gly623=
ENST00000681190.1:c.1869G>A ENSP00000506428.1:p.Gly623=
ENST00000681874.1:c.1869G>A ENSP00000505162.1:p.Gly623=
ENST00000362061.3:c.1869G>A ENSP00000355192.3:p.Gly623=
ENST00000367338.7:c.1869G>A ENSP00000356307.3:p.Gly623=
NM_000069.2:c.1869G>A NP_000060.2:p.Gly623=
XM_005245478.2:c.1869G>A XP_005245535.1:p.Gly623=
XM_005245478.3:c.1869G>A XP_005245535.1:p.Gly623=
NM_000069.3:c.1869G>A MANE Select NP_000060.2:p.Gly623=