Canonical Allele Identifier: CA083650
Gene: CACNA1S HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201043333C>T , CM000663.2:g.201043333C>T GRCh38
NC_000001.10:g.201012461C>T , CM000663.1:g.201012461C>T GRCh37
NC_000001.9:g.199279084C>T NCBI36
NG_009816.1:g.74234G>A
NG_009816.2:g.74234G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000362061.4:c.4996G>A MANE Select ENSP00000355192.3:p.Ala1666Thr
ENST00000679417.1:c.*4159G>A ENSP00000506706.1:n.*4159G>A
ENST00000680051.1:n.2122G>A
ENST00000680059.1:c.*2514G>A ENSP00000504944.1:n.*2514G>A
ENST00000681078.1:c.*771G>A ENSP00000506645.1:n.*771G>A
ENST00000681190.1:c.*1178G>A ENSP00000506428.1:n.*1178G>A
ENST00000681874.1:c.4936G>A ENSP00000505162.1:p.Ala1646Thr
ENST00000362061.3:c.4996G>A ENSP00000355192.3:p.Ala1666Thr
ENST00000367338.7:c.4939G>A ENSP00000356307.3:p.Ala1647Thr
NM_000069.2:c.4996G>A NP_000060.2:p.Ala1666Thr
XM_005245478.2:c.4939G>A XP_005245535.1:p.Ala1647Thr
XM_005245478.3:c.4939G>A XP_005245535.1:p.Ala1647Thr
NM_000069.3:c.4996G>A MANE Select NP_000060.2:p.Ala1666Thr