Canonical Allele Identifier: CA344119519

Gene: CACNA1S

Linked Data

• MyVariant Identifiers: chr1:g.201046071G>A (hg19) ; chr1:g.201076943G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201076943G>A , CM000663.2:g.201076943G>A	GRCh38
NC_000001.10:g.201046071G>A , CM000663.1:g.201046071G>A	GRCh37
NC_000001.9:g.199312694G>A	NCBI36
NG_009816.1:g.40624C>T
NG_009816.2:g.40624C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000362061.4:c.1804C>T MANE Select	ENSP00000355192.3:p.Gln602Ter
ENST00000679417.1:c.*967C>T	ENSP00000506706.1:n.*967C>T
ENST00000680059.1:c.1804C>T	ENSP00000504944.1:p.Gln602Ter
ENST00000681078.1:c.1804C>T	ENSP00000506645.1:p.Gln602Ter
ENST00000681190.1:c.1804C>T	ENSP00000506428.1:p.Gln602Ter
ENST00000681874.1:c.1804C>T	ENSP00000505162.1:p.Gln602Ter
ENST00000362061.3:c.1804C>T	ENSP00000355192.3:p.Gln602Ter
ENST00000367338.7:c.1804C>T	ENSP00000356307.3:p.Gln602Ter
NM_000069.2:c.1804C>T	NP_000060.2:p.Gln602Ter
XM_005245478.2:c.1804C>T	XP_005245535.1:p.Gln602Ter
XM_005245478.3:c.1804C>T	XP_005245535.1:p.Gln602Ter
NM_000069.3:c.1804C>T MANE Select	NP_000060.2:p.Gln602Ter