Canonical Allele Identifier: CA36006607

Gene: CACNA1S

Linked Data

• dbSNP Id: rs775967225
• gnomAD v4: 1-201060525-G-A
• MyVariant Identifiers: chr1:g.201029653G>A (hg19) ; chr1:g.201060525G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201060525G>A , CM000663.2:g.201060525G>A	GRCh38
NC_000001.10:g.201029653G>A , CM000663.1:g.201029653G>A	GRCh37
NC_000001.9:g.199296276G>A	NCBI36
NG_009816.1:g.57042C>T
NG_009816.2:g.57042C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000362061.4:c.3414+133C>T MANE Select	ENSP00000355192.3:n.3414+133C>T
ENST00000679417.1:c.*2577+133C>T	ENSP00000506706.1:n.*2577+133C>T
ENST00000680051.1:n.540+133C>T
ENST00000680059.1:c.*932+133C>T	ENSP00000504944.1:n.*932+133C>T
ENST00000681078.1:c.3414+133C>T	ENSP00000506645.1:n.3414+133C>T
ENST00000681190.1:c.3414+133C>T	ENSP00000506428.1:n.3414+133C>T
ENST00000681874.1:c.3354+133C>T	ENSP00000505162.1:n.3354+133C>T
ENST00000362061.3:c.3414+133C>T	ENSP00000355192.3:n.3414+133C>T
ENST00000367338.7:c.3414+133C>T	ENSP00000356307.3:n.3414+133C>T
NM_000069.2:c.3414+133C>T	NP_000060.2:n.3414+133C>T
XM_005245478.2:c.3414+133C>T	XP_005245535.1:n.3414+133C>T
XM_005245478.3:c.3414+133C>T	XP_005245535.1:n.3414+133C>T
NM_000069.3:c.3414+133C>T MANE Select	NP_000060.2:n.3414+133C>T