Canonical Allele Identifier: CA344101247

Gene: CACNA1S

Linked Data

• ClinVar Variation Id: 3026715
• ClinVar RCV Id: RCV003887108
• dbSNP Id: rs76460090
• MyVariant Identifiers: chr1:g.201034980C>A (hg19) ; chr1:g.201065852C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201065852C>A , CM000663.2:g.201065852C>A	GRCh38
NC_000001.10:g.201034980C>A , CM000663.1:g.201034980C>A	GRCh37
NC_000001.9:g.199301603C>A	NCBI36
NG_009816.1:g.51715G>T
NG_009816.2:g.51715G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362061.4:c.2839G>T MANE Select	ENSP00000355192.3:p.Val947Phe
ENST00000679417.1:c.*2002G>T	ENSP00000506706.1:n.*2002G>T
ENST00000680059.1:c.*357G>T	ENSP00000504944.1:n.*357G>T
ENST00000681078.1:c.2839G>T	ENSP00000506645.1:p.Val947Phe
ENST00000681190.1:c.2839G>T	ENSP00000506428.1:p.Val947Phe
ENST00000681874.1:c.2779G>T	ENSP00000505162.1:p.Val927Phe
ENST00000362061.3:c.2839G>T	ENSP00000355192.3:p.Val947Phe
ENST00000367338.7:c.2839G>T	ENSP00000356307.3:p.Val947Phe
NM_000069.2:c.2839G>T	NP_000060.2:p.Val947Phe
XM_005245478.2:c.2839G>T	XP_005245535.1:p.Val947Phe
XM_005245478.3:c.2839G>T	XP_005245535.1:p.Val947Phe
NM_000069.3:c.2839G>T MANE Select	NP_000060.2:p.Val947Phe