Canonical Allele Identifier: CA1320966749
Gene: CASP10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201208077G= , CM000664.2:g.201208077G= GRCh38
NC_000002.11:g.202072800G= , CM000664.1:g.202072800G= GRCh37
NC_000002.10:g.201781045G= NCBI36
NG_007265.1:g.29946G= , LRG_33:g.29946G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000313728.12:c.722-993G= ENSP00000314599.7:n.722-993G=
ENST00000346817.10:c.687G= ENSP00000237865.7:p.Arg229=
ENST00000438843.6:c.*273G= ENSP00000401914.1:n.*273G=
ENST00000492363.6:c.724G= ENSP00000512459.1:p.Gly242=
ENST00000696199.1:c.721+4311G= ENSP00000512481.1:n.721+4311G=
ENST00000286186.11:c.816G= MANE Select ENSP00000286186.6:p.Arg272=
ENST00000272879.9:c.816G= ENSP00000272879.5:p.Arg272=
ENST00000286186.10:c.816G= ENSP00000286186.6:p.Arg272=
ENST00000313728.11:c.722-993G= ENSP00000314599.7:n.722-993G=
ENST00000346817.9:c.687G= ENSP00000237865.7:p.Arg229=
ENST00000360132.7:c.724G= ENSP00000353250.3:p.Gly242=
ENST00000438843.5:c.*273G= ENSP00000401914.1:n.*273G=
ENST00000448480.1:c.687G= ENSP00000396835.1:p.Arg229=
ENST00000492363.5:n.724G=
NM_001206524.1:c.722-993G= NP_001193453.1:n.722-993G=
NM_001206542.1:c.687G= NP_001193471.1:p.Arg229=
NM_001230.4:c.687G= NP_001221.2:p.Arg229=
NM_032974.4:c.816G= NP_116756.2:p.Arg272=
NM_032976.3:c.724G= NP_116758.1:p.Gly242=
NM_032977.3:c.816G= , LRG_33t1:c.816G= NP_116759.2:p.Arg272=
XM_005246907.2:c.813G= XP_005246964.1:p.Arg271=
XM_006712796.2:c.66G= XP_006712859.1:p.Arg22=
XM_011511990.1:c.721G= XP_011510292.1:p.Gly241=
XR_923043.1:n.1020G=
XR_923044.1:n.928G=
XM_006712796.3:c.66G= XP_006712859.1:p.Arg22=
XM_011511990.2:c.721G= XP_011510292.1:p.Gly241=
XR_923043.2:n.1020G=
XR_923044.2:n.928G=
NM_001206524.2:c.722-993G= NP_001193453.1:n.722-993G=
NM_001206542.2:c.687G= NP_001193471.1:p.Arg229=
NM_001230.5:c.687G= NP_001221.2:p.Arg229=
NM_032974.5:c.816G= NP_116756.2:p.Arg272=
NM_032977.4:c.816G= MANE Select NP_116759.2:p.Arg272=
NM_032976.4:c.724G= NP_116758.1:p.Gly242=