Canonical Allele Identifier: CA344121065

Gene: CACNA1S

Linked Data

• MyVariant Identifiers: chr1:g.201047013A>G (hg19) ; chr1:g.201077885A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201077885A>G , CM000663.2:g.201077885A>G	GRCh38
NC_000001.10:g.201047013A>G , CM000663.1:g.201047013A>G	GRCh37
NC_000001.9:g.199313636A>G	NCBI36
NG_009816.1:g.39682T>C
NG_009816.2:g.39682T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362061.4:c.1613T>C MANE Select	ENSP00000355192.3:p.Ile538Thr
ENST00000679417.1:c.*776T>C	ENSP00000506706.1:n.*776T>C
ENST00000680059.1:c.1613T>C	ENSP00000504944.1:p.Ile538Thr
ENST00000681078.1:c.1613T>C	ENSP00000506645.1:p.Ile538Thr
ENST00000681190.1:c.1613T>C	ENSP00000506428.1:p.Ile538Thr
ENST00000681874.1:c.1613T>C	ENSP00000505162.1:p.Ile538Thr
ENST00000362061.3:c.1613T>C	ENSP00000355192.3:p.Ile538Thr
ENST00000367338.7:c.1613T>C	ENSP00000356307.3:p.Ile538Thr
NM_000069.2:c.1613T>C	NP_000060.2:p.Ile538Thr
XM_005245478.2:c.1613T>C	XP_005245535.1:p.Ile538Thr
XM_005245478.3:c.1613T>C	XP_005245535.1:p.Ile538Thr
NM_000069.3:c.1613T>C MANE Select	NP_000060.2:p.Ile538Thr