Canonical Allele Identifier: CA344157300

Gene: CACNA1S

Linked Data

• MyVariant Identifiers: chr1:g.201027537T>A (hg19) ; chr1:g.201058409T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201058409T>A , CM000663.2:g.201058409T>A	GRCh38
NC_000001.10:g.201027537T>A , CM000663.1:g.201027537T>A	GRCh37
NC_000001.9:g.199294160T>A	NCBI36
NG_009816.1:g.59158A>T
NG_009816.2:g.59158A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000362061.4:c.3608A>T MANE Select	ENSP00000355192.3:p.Asp1203Val
ENST00000679417.1:c.*2771A>T	ENSP00000506706.1:n.*2771A>T
ENST00000680051.1:n.734A>T
ENST00000680059.1:c.*1126A>T	ENSP00000504944.1:n.*1126A>T
ENST00000681078.1:c.3608A>T	ENSP00000506645.1:p.Asp1203Val
ENST00000681190.1:c.3608A>T	ENSP00000506428.1:p.Asp1203Val
ENST00000681874.1:c.3548A>T	ENSP00000505162.1:p.Asp1183Val
ENST00000362061.3:c.3608A>T	ENSP00000355192.3:p.Asp1203Val
ENST00000367338.7:c.3608A>T	ENSP00000356307.3:p.Asp1203Val
NM_000069.2:c.3608A>T	NP_000060.2:p.Asp1203Val
XM_005245478.2:c.3608A>T	XP_005245535.1:p.Asp1203Val
XM_005245478.3:c.3608A>T	XP_005245535.1:p.Asp1203Val
NM_000069.3:c.3608A>T MANE Select	NP_000060.2:p.Asp1203Val