Canonical Allele Identifier: CA344149998

Gene: CACNA1S

Linked Data

• MyVariant Identifiers: chr1:g.201020164G>C (hg19) ; chr1:g.201051036G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201051036G>C , CM000663.2:g.201051036G>C	GRCh38
NC_000001.10:g.201020164G>C , CM000663.1:g.201020164G>C	GRCh37
NC_000001.9:g.199286787G>C	NCBI36
NG_009816.1:g.66531C>G
NG_009816.2:g.66531C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362061.4:c.4061C>G MANE Select	ENSP00000355192.3:p.Thr1354Ser
ENST00000679417.1:c.*3224C>G	ENSP00000506706.1:n.*3224C>G
ENST00000680051.1:n.1187C>G
ENST00000680059.1:c.*1579C>G	ENSP00000504944.1:n.*1579C>G
ENST00000681078.1:c.4061C>G	ENSP00000506645.1:p.Thr1354Ser
ENST00000681190.1:c.*243C>G	ENSP00000506428.1:n.*243C>G
ENST00000681874.1:c.4001C>G	ENSP00000505162.1:p.Thr1334Ser
ENST00000362061.3:c.4061C>G	ENSP00000355192.3:p.Thr1354Ser
ENST00000367338.7:c.4004C>G	ENSP00000356307.3:p.Thr1335Ser
NM_000069.2:c.4061C>G	NP_000060.2:p.Thr1354Ser
XM_005245478.2:c.4004C>G	XP_005245535.1:p.Thr1335Ser
XM_005245478.3:c.4004C>G	XP_005245535.1:p.Thr1335Ser
NM_000069.3:c.4061C>G MANE Select	NP_000060.2:p.Thr1354Ser