Canonical Allele Identifier: CA1219585314
Gene: CACNA1S HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201078282_201078283delinsCA , CM000663.2:g.201078282_201078283delinsCA GRCh38
NC_000001.10:g.201047410_201047411delinsCA , CM000663.1:g.201047410_201047411delinsCA GRCh37
NC_000001.9:g.199314033_199314034delinsCA NCBI36
NG_009816.1:g.39284_39285delinsTG
NG_009816.2:g.39284_39285delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000362061.4:c.1394-179_1394-178delinsTG MANE Select ENSP00000355192.3:n.1394-179_1394-178delinsTG
ENST00000679417.1:c.*557-179_*557-178delinsTG ENSP00000506706.1:n.*557-179_*557-178delinsTG
ENST00000680059.1:c.1394-179_1394-178delinsTG ENSP00000504944.1:n.1394-179_1394-178delinsTG
ENST00000681078.1:c.1394-179_1394-178delinsTG ENSP00000506645.1:n.1394-179_1394-178delinsTG
ENST00000681190.1:c.1394-179_1394-178delinsTG ENSP00000506428.1:n.1394-179_1394-178delinsTG
ENST00000681874.1:c.1394-179_1394-178delinsTG ENSP00000505162.1:n.1394-179_1394-178delinsTG
ENST00000362061.3:c.1394-179_1394-178delinsTG ENSP00000355192.3:n.1394-179_1394-178delinsTG
ENST00000367338.7:c.1394-179_1394-178delinsTG ENSP00000356307.3:n.1394-179_1394-178delinsTG
NM_000069.2:c.1394-179_1394-178delinsTG NP_000060.2:n.1394-179_1394-178delinsTG
XM_005245478.2:c.1394-179_1394-178delinsTG XP_005245535.1:n.1394-179_1394-178delinsTG
XM_005245478.3:c.1394-179_1394-178delinsTG XP_005245535.1:n.1394-179_1394-178delinsTG
NM_000069.3:c.1394-179_1394-178delinsTG MANE Select NP_000060.2:n.1394-179_1394-178delinsTG