Canonical Allele Identifier: CA422814901
Gene: CACNA1S HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.201047021G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201077893G>A , CM000663.2:g.201077893G>A GRCh38
NC_000001.10:g.201047021G>A , CM000663.1:g.201047021G>A GRCh37
NC_000001.9:g.199313644G>A NCBI36
NG_009816.1:g.39674C>T
NG_009816.2:g.39674C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000362061.4:c.1605C>T MANE Select ENSP00000355192.3:p.Ile535=
ENST00000679417.1:c.*768C>T ENSP00000506706.1:n.*768C>T
ENST00000680059.1:c.1605C>T ENSP00000504944.1:p.Ile535=
ENST00000681078.1:c.1605C>T ENSP00000506645.1:p.Ile535=
ENST00000681190.1:c.1605C>T ENSP00000506428.1:p.Ile535=
ENST00000681874.1:c.1605C>T ENSP00000505162.1:p.Ile535=
ENST00000362061.3:c.1605C>T ENSP00000355192.3:p.Ile535=
ENST00000367338.7:c.1605C>T ENSP00000356307.3:p.Ile535=
NM_000069.2:c.1605C>T NP_000060.2:p.Ile535=
XM_005245478.2:c.1605C>T XP_005245535.1:p.Ile535=
XM_005245478.3:c.1605C>T XP_005245535.1:p.Ile535=
NM_000069.3:c.1605C>T MANE Select NP_000060.2:p.Ile535=