Canonical Allele Identifier: CA344157477
Gene: CACNA1S HGNC NCBI

Linked Data

dbSNP Id: rs1414905226

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201058442C>A , CM000663.2:g.201058442C>A GRCh38
NC_000001.10:g.201027570C>A , CM000663.1:g.201027570C>A GRCh37
NC_000001.9:g.199294193C>A NCBI36
NG_009816.1:g.59125G>T
NG_009816.2:g.59125G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000362061.4:c.3575G>T MANE Select ENSP00000355192.3:p.Gly1192Val
ENST00000679417.1:c.*2738G>T ENSP00000506706.1:n.*2738G>T
ENST00000680051.1:n.701G>T
ENST00000680059.1:c.*1093G>T ENSP00000504944.1:n.*1093G>T
ENST00000681078.1:c.3575G>T ENSP00000506645.1:p.Gly1192Val
ENST00000681190.1:c.3575G>T ENSP00000506428.1:p.Gly1192Val
ENST00000681874.1:c.3515G>T ENSP00000505162.1:p.Gly1172Val
ENST00000362061.3:c.3575G>T ENSP00000355192.3:p.Gly1192Val
ENST00000367338.7:c.3575G>T ENSP00000356307.3:p.Gly1192Val
NM_000069.2:c.3575G>T NP_000060.2:p.Gly1192Val
XM_005245478.2:c.3575G>T XP_005245535.1:p.Gly1192Val
XM_005245478.3:c.3575G>T XP_005245535.1:p.Gly1192Val
NM_000069.3:c.3575G>T MANE Select NP_000060.2:p.Gly1192Val