Canonical Allele Identifier: CA730085522

Gene: CACNA1S

Linked Data

• dbSNP Id: rs1378673677
• MyVariant Identifiers: chr1:g.201045862A>C (hg19) ; chr1:g.201076734A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201076734A>C , CM000663.2:g.201076734A>C	GRCh38
NC_000001.10:g.201045862A>C , CM000663.1:g.201045862A>C	GRCh37
NC_000001.9:g.199312485A>C	NCBI36
NG_009816.1:g.40833T>G
NG_009816.2:g.40833T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362061.4:c.1827+186T>G MANE Select	ENSP00000355192.3:n.1827+186T>G
ENST00000679417.1:c.*990+186T>G	ENSP00000506706.1:n.*990+186T>G
ENST00000680059.1:c.1827+186T>G	ENSP00000504944.1:n.1827+186T>G
ENST00000681078.1:c.1827+186T>G	ENSP00000506645.1:n.1827+186T>G
ENST00000681190.1:c.1827+186T>G	ENSP00000506428.1:n.1827+186T>G
ENST00000681874.1:c.1827+186T>G	ENSP00000505162.1:n.1827+186T>G
ENST00000362061.3:c.1827+186T>G	ENSP00000355192.3:n.1827+186T>G
ENST00000367338.7:c.1827+186T>G	ENSP00000356307.3:n.1827+186T>G
NM_000069.2:c.1827+186T>G	NP_000060.2:n.1827+186T>G
XM_005245478.2:c.1827+186T>G	XP_005245535.1:n.1827+186T>G
XM_005245478.3:c.1827+186T>G	XP_005245535.1:n.1827+186T>G
NM_000069.3:c.1827+186T>G MANE Select	NP_000060.2:n.1827+186T>G