Canonical Allele Identifier: CA1320966752

Gene: CASP10

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201208085T= , CM000664.2:g.201208085T=	GRCh38
NC_000002.11:g.202072808T= , CM000664.1:g.202072808T=	GRCh37
NC_000002.10:g.201781053T=	NCBI36
NG_007265.1:g.29954T= , LRG_33:g.29954T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313728.12:c.722-985T=	ENSP00000314599.7:n.722-985T=
ENST00000346817.10:c.695T=	ENSP00000237865.7:p.Val232=
ENST00000438843.6:c.*281T=	ENSP00000401914.1:n.*281T=
ENST00000492363.6:c.732T=	ENSP00000512459.1:p.Cys244=
ENST00000696199.1:c.721+4319T=	ENSP00000512481.1:n.721+4319T=
ENST00000286186.11:c.824T= MANE Select	ENSP00000286186.6:p.Val275=
ENST00000272879.9:c.824T=	ENSP00000272879.5:p.Val275=
ENST00000286186.10:c.824T=	ENSP00000286186.6:p.Val275=
ENST00000313728.11:c.722-985T=	ENSP00000314599.7:n.722-985T=
ENST00000346817.9:c.695T=	ENSP00000237865.7:p.Val232=
ENST00000360132.7:c.732T=	ENSP00000353250.3:p.Cys244=
ENST00000438843.5:c.*281T=	ENSP00000401914.1:n.*281T=
ENST00000448480.1:c.695T=	ENSP00000396835.1:p.Val232=
ENST00000492363.5:n.732T=
NM_001206524.1:c.722-985T=	NP_001193453.1:n.722-985T=
NM_001206542.1:c.695T=	NP_001193471.1:p.Val232=
NM_001230.4:c.695T=	NP_001221.2:p.Val232=
NM_032974.4:c.824T=	NP_116756.2:p.Val275=
NM_032976.3:c.732T=	NP_116758.1:p.Cys244=
NM_032977.3:c.824T= , LRG_33t1:c.824T=	NP_116759.2:p.Val275=
XM_005246907.2:c.821T=	XP_005246964.1:p.Val274=
XM_006712796.2:c.74T=	XP_006712859.1:p.Val25=
XM_011511990.1:c.729T=	XP_011510292.1:p.Cys243=
XR_923043.1:n.1028T=
XR_923044.1:n.936T=
XM_006712796.3:c.74T=	XP_006712859.1:p.Val25=
XM_011511990.2:c.729T=	XP_011510292.1:p.Cys243=
XR_923043.2:n.1028T=
XR_923044.2:n.936T=
NM_001206524.2:c.722-985T=	NP_001193453.1:n.722-985T=
NM_001206542.2:c.695T=	NP_001193471.1:p.Val232=
NM_001230.5:c.695T=	NP_001221.2:p.Val232=
NM_032974.5:c.824T=	NP_116756.2:p.Val275=
NM_032977.4:c.824T= MANE Select	NP_116759.2:p.Val275=
NM_032976.4:c.732T=	NP_116758.1:p.Cys244=