Canonical Allele Identifier: CA1219585090
Gene: CACNA1S HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201077757G= , CM000663.2:g.201077757G= GRCh38
NC_000001.10:g.201046885G= , CM000663.1:g.201046885G= GRCh37
NC_000001.9:g.199313508G= NCBI36
NG_009816.1:g.39810C=
NG_009816.2:g.39810C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000362061.4:c.1619+122C= MANE Select ENSP00000355192.3:n.1619+122C=
ENST00000679417.1:c.*782+122C= ENSP00000506706.1:n.*782+122C=
ENST00000680059.1:c.1619+122C= ENSP00000504944.1:n.1619+122C=
ENST00000681078.1:c.1619+122C= ENSP00000506645.1:n.1619+122C=
ENST00000681190.1:c.1619+122C= ENSP00000506428.1:n.1619+122C=
ENST00000681874.1:c.1619+122C= ENSP00000505162.1:n.1619+122C=
ENST00000362061.3:c.1619+122C= ENSP00000355192.3:n.1619+122C=
ENST00000367338.7:c.1619+122C= ENSP00000356307.3:n.1619+122C=
NM_000069.2:c.1619+122C= NP_000060.2:n.1619+122C=
XM_005245478.2:c.1619+122C= XP_005245535.1:n.1619+122C=
XM_005245478.3:c.1619+122C= XP_005245535.1:n.1619+122C=
NM_000069.3:c.1619+122C= MANE Select NP_000060.2:n.1619+122C=