Canonical Allele Identifier: CA1320967298
Gene: CASP10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201209270C= , CM000664.2:g.201209270C= GRCh38
NC_000002.11:g.202073993C= , CM000664.1:g.202073993C= GRCh37
NC_000002.10:g.201782238C= NCBI36
NG_007265.1:g.31139C= , LRG_33:g.31139C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000313728.12:c.922C= ENSP00000314599.7:p.Arg308=
ENST00000346817.10:c.994C= ENSP00000237865.7:p.Arg332=
ENST00000438843.6:c.*580C= ENSP00000401914.1:n.*580C=
ENST00000492363.6:c.*209C= ENSP00000512459.1:n.*209C=
ENST00000696199.1:c.721+5504C= ENSP00000512481.1:n.721+5504C=
ENST00000286186.11:c.1123C= MANE Select ENSP00000286186.6:p.Arg375=
ENST00000272879.9:c.1123C= ENSP00000272879.5:p.Arg375=
ENST00000286186.10:c.1123C= ENSP00000286186.6:p.Arg375=
ENST00000313728.11:c.922C= ENSP00000314599.7:p.Arg308=
ENST00000346817.9:c.994C= ENSP00000237865.7:p.Arg332=
ENST00000360132.7:c.*209C= ENSP00000353250.3:n.*209C=
ENST00000448480.1:c.994C= ENSP00000396835.1:p.Arg332=
ENST00000492363.5:n.1031C=
NM_001206524.1:c.922C= NP_001193453.1:p.Arg308=
NM_001206542.1:c.994C= NP_001193471.1:p.Arg332=
NM_001230.4:c.994C= NP_001221.2:p.Arg332=
NM_032974.4:c.1123C= NP_116756.2:p.Arg375=
NM_032976.3:c.*209C= NP_116758.1:n.*209C=
NM_032977.3:c.1123C= , LRG_33t1:c.1123C= NP_116759.2:p.Arg375=
XM_005246907.2:c.1120C= XP_005246964.1:p.Arg374=
XM_006712796.2:c.373C= XP_006712859.1:p.Arg125=
XM_006712796.3:c.373C= XP_006712859.1:p.Arg125=
NM_001206524.2:c.922C= NP_001193453.1:p.Arg308=
NM_001206542.2:c.994C= NP_001193471.1:p.Arg332=
NM_001230.5:c.994C= NP_001221.2:p.Arg332=
NM_032974.5:c.1123C= NP_116756.2:p.Arg375=
NM_032977.4:c.1123C= MANE Select NP_116759.2:p.Arg375=
NM_032976.4:c.*209C= NP_116758.1:n.*209C=