Canonical Allele Identifier: CA2531234331
Gene: CACNA1S HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201058759G>T , CM000663.2:g.201058759G>T GRCh38
NC_000001.10:g.201027887G>T , CM000663.1:g.201027887G>T GRCh37
NC_000001.9:g.199294510G>T NCBI36
NG_009816.1:g.58808C>A
NG_009816.2:g.58808C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000362061.4:c.3526-268C>A MANE Select ENSP00000355192.3:n.3526-268C>A
ENST00000679417.1:c.*2689-268C>A ENSP00000506706.1:n.*2689-268C>A
ENST00000680051.1:n.652-268C>A
ENST00000680059.1:c.*1044-268C>A ENSP00000504944.1:n.*1044-268C>A
ENST00000681078.1:c.3526-268C>A ENSP00000506645.1:n.3526-268C>A
ENST00000681190.1:c.3526-268C>A ENSP00000506428.1:n.3526-268C>A
ENST00000681874.1:c.3466-268C>A ENSP00000505162.1:n.3466-268C>A
ENST00000362061.3:c.3526-268C>A ENSP00000355192.3:n.3526-268C>A
ENST00000367338.7:c.3526-268C>A ENSP00000356307.3:n.3526-268C>A
NM_000069.2:c.3526-268C>A NP_000060.2:n.3526-268C>A
XM_005245478.2:c.3526-268C>A XP_005245535.1:n.3526-268C>A
XM_005245478.3:c.3526-268C>A XP_005245535.1:n.3526-268C>A
NM_000069.3:c.3526-268C>A MANE Select NP_000060.2:n.3526-268C>A