Canonical Allele Identifier: CA2747336672
Gene: CACNA1S HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201075458_201075459insCAAAC , CM000663.2:g.201075458_201075459insCAAAC GRCh38
NC_000001.10:g.201044586_201044587insCAAAC , CM000663.1:g.201044586_201044587insCAAAC GRCh37
NC_000001.9:g.199311209_199311210insCAAAC NCBI36
NG_009816.1:g.42109_42110insTTTGG
NG_009816.2:g.42109_42110insTTTGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000362061.4:c.1948+37_1948+38insTTTGG MANE Select ENSP00000355192.3:n.1948+37_1948+38insTTTGG
ENST00000679417.1:c.*1111+37_*1111+38insTTTGG ENSP00000506706.1:n.*1111+37_*1111+38insTTTGG
ENST00000680059.1:c.1948+37_1948+38insTTTGG ENSP00000504944.1:n.1948+37_1948+38insTTTGG
ENST00000681078.1:c.1948+37_1948+38insTTTGG ENSP00000506645.1:n.1948+37_1948+38insTTTGG
ENST00000681190.1:c.1948+37_1948+38insTTTGG ENSP00000506428.1:n.1948+37_1948+38insTTTGG
ENST00000681874.1:c.1948+37_1948+38insTTTGG ENSP00000505162.1:n.1948+37_1948+38insTTTGG
ENST00000362061.3:c.1948+37_1948+38insTTTGG ENSP00000355192.3:n.1948+37_1948+38insTTTGG
ENST00000367338.7:c.1948+37_1948+38insTTTGG ENSP00000356307.3:n.1948+37_1948+38insTTTGG
NM_000069.2:c.1948+37_1948+38insTTTGG NP_000060.2:n.1948+37_1948+38insTTTGG
XM_005245478.2:c.1948+37_1948+38insTTTGG XP_005245535.1:n.1948+37_1948+38insTTTGG
XM_005245478.3:c.1948+37_1948+38insTTTGG XP_005245535.1:n.1948+37_1948+38insTTTGG
NM_000069.3:c.1948+37_1948+38insTTTGG MANE Select NP_000060.2:n.1948+37_1948+38insTTTGG