Canonical Allele Identifier: CA2649766143

Gene: CACNA1S

Linked Data

• gnomAD v4: 1-201076782-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201076782C>A , CM000663.2:g.201076782C>A	GRCh38
NC_000001.10:g.201045910C>A , CM000663.1:g.201045910C>A	GRCh37
NC_000001.9:g.199312533C>A	NCBI36
NG_009816.1:g.40785G>T
NG_009816.2:g.40785G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362061.4:c.1827+138G>T MANE Select	ENSP00000355192.3:n.1827+138G>T
ENST00000679417.1:c.*990+138G>T	ENSP00000506706.1:n.*990+138G>T
ENST00000680059.1:c.1827+138G>T	ENSP00000504944.1:n.1827+138G>T
ENST00000681078.1:c.1827+138G>T	ENSP00000506645.1:n.1827+138G>T
ENST00000681190.1:c.1827+138G>T	ENSP00000506428.1:n.1827+138G>T
ENST00000681874.1:c.1827+138G>T	ENSP00000505162.1:n.1827+138G>T
ENST00000362061.3:c.1827+138G>T	ENSP00000355192.3:n.1827+138G>T
ENST00000367338.7:c.1827+138G>T	ENSP00000356307.3:n.1827+138G>T
NM_000069.2:c.1827+138G>T	NP_000060.2:n.1827+138G>T
XM_005245478.2:c.1827+138G>T	XP_005245535.1:n.1827+138G>T
XM_005245478.3:c.1827+138G>T	XP_005245535.1:n.1827+138G>T
NM_000069.3:c.1827+138G>T MANE Select	NP_000060.2:n.1827+138G>T