Canonical Allele Identifier: CA344138794

Gene: CACNA1S

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201044327C>T , CM000663.2:g.201044327C>T	GRCh38
NC_000001.10:g.201013455C>T , CM000663.1:g.201013455C>T	GRCh37
NC_000001.9:g.199280078C>T	NCBI36
NG_009816.1:g.73240G>A
NG_009816.2:g.73240G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000069.3:c.4797+1G>A MANE Select	NP_000060.2:n.4797+1G>A
ENST00000362061.4:c.4797+1G>A MANE Select	ENSP00000355192.3:n.4797+1G>A
NM_000069.2:c.4797+1G>A	NP_000060.2:n.4797+1G>A
ENST00000362061.3:c.4797+1G>A	ENSP00000355192.3:n.4797+1G>A
ENST00000367338.7:c.4740+1G>A	ENSP00000356307.3:n.4740+1G>A
ENST00000679417.1:c.*3960+1G>A	ENSP00000506706.1:n.*3960+1G>A
ENST00000680051.1:n.1923+1G>A
ENST00000680059.1:c.*2315+1G>A	ENSP00000504944.1:n.*2315+1G>A
ENST00000681078.1:c.*572+1G>A	ENSP00000506645.1:n.*572+1G>A
ENST00000681190.1:c.*979+1G>A	ENSP00000506428.1:n.*979+1G>A
ENST00000681874.1:c.4737+1G>A	ENSP00000505162.1:n.4737+1G>A
XM_005245478.2:c.4740+1G>A	XP_005245535.1:n.4740+1G>A
XM_005245478.3:c.4740+1G>A	XP_005245535.1:n.4740+1G>A