Canonical Allele Identifier: CA1219584753
Gene: CACNA1S HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201076950_201076951delinsGT , CM000663.2:g.201076950_201076951delinsGT GRCh38
NC_000001.10:g.201046078_201046079delinsGT , CM000663.1:g.201046078_201046079delinsGT GRCh37
NC_000001.9:g.199312701_199312702delinsGT NCBI36
NG_009816.1:g.40616_40617delinsAC
NG_009816.2:g.40616_40617delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000362061.4:c.1796_1797delinsAC MANE Select ENSP00000355192.3:p.Asn599=
ENST00000679417.1:c.*959_*960delinsAC ENSP00000506706.1:n.*959_*960delinsAC
ENST00000680059.1:c.1796_1797delinsAC ENSP00000504944.1:p.Asn599=
ENST00000681078.1:c.1796_1797delinsAC ENSP00000506645.1:p.Asn599=
ENST00000681190.1:c.1796_1797delinsAC ENSP00000506428.1:p.Asn599=
ENST00000681874.1:c.1796_1797delinsAC ENSP00000505162.1:p.Asn599=
ENST00000362061.3:c.1796_1797delinsAC ENSP00000355192.3:p.Asn599=
ENST00000367338.7:c.1796_1797delinsAC ENSP00000356307.3:p.Asn599=
NM_000069.2:c.1796_1797delinsAC NP_000060.2:p.Asn599=
XM_005245478.2:c.1796_1797delinsAC XP_005245535.1:p.Asn599=
XM_005245478.3:c.1796_1797delinsAC XP_005245535.1:p.Asn599=
NM_000069.3:c.1796_1797delinsAC MANE Select NP_000060.2:p.Asn599=