Canonical Allele Identifier: CA1320966760

Gene: CASP10

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201208106A= , CM000664.2:g.201208106A=	GRCh38
NC_000002.11:g.202072829A= , CM000664.1:g.202072829A=	GRCh37
NC_000002.10:g.201781074A=	NCBI36
NG_007265.1:g.29975A= , LRG_33:g.29975A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313728.12:c.722-964A=	ENSP00000314599.7:n.722-964A=
ENST00000346817.10:c.716A=	ENSP00000237865.7:p.His239=
ENST00000438843.6:c.*302A=	ENSP00000401914.1:n.*302A=
ENST00000492363.6:c.753A=	ENSP00000512459.1:p.Pro251=
ENST00000696199.1:c.721+4340A=	ENSP00000512481.1:n.721+4340A=
ENST00000286186.11:c.845A= MANE Select	ENSP00000286186.6:p.His282=
ENST00000272879.9:c.845A=	ENSP00000272879.5:p.His282=
ENST00000286186.10:c.845A=	ENSP00000286186.6:p.His282=
ENST00000313728.11:c.722-964A=	ENSP00000314599.7:n.722-964A=
ENST00000346817.9:c.716A=	ENSP00000237865.7:p.His239=
ENST00000360132.7:c.753A=	ENSP00000353250.3:p.Pro251=
ENST00000438843.5:c.*302A=	ENSP00000401914.1:n.*302A=
ENST00000448480.1:c.716A=	ENSP00000396835.1:p.His239=
ENST00000492363.5:n.753A=
NM_001206524.1:c.722-964A=	NP_001193453.1:n.722-964A=
NM_001206542.1:c.716A=	NP_001193471.1:p.His239=
NM_001230.4:c.716A=	NP_001221.2:p.His239=
NM_032974.4:c.845A=	NP_116756.2:p.His282=
NM_032976.3:c.753A=	NP_116758.1:p.Pro251=
NM_032977.3:c.845A= , LRG_33t1:c.845A=	NP_116759.2:p.His282=
XM_005246907.2:c.842A=	XP_005246964.1:p.His281=
XM_006712796.2:c.95A=	XP_006712859.1:p.His32=
XM_011511990.1:c.750A=	XP_011510292.1:p.Pro250=
XR_923043.1:n.1049A=
XR_923044.1:n.957A=
XM_006712796.3:c.95A=	XP_006712859.1:p.His32=
XM_011511990.2:c.750A=	XP_011510292.1:p.Pro250=
XR_923043.2:n.1049A=
XR_923044.2:n.957A=
NM_001206524.2:c.722-964A=	NP_001193453.1:n.722-964A=
NM_001206542.2:c.716A=	NP_001193471.1:p.His239=
NM_001230.5:c.716A=	NP_001221.2:p.His239=
NM_032974.5:c.845A=	NP_116756.2:p.His282=
NM_032977.4:c.845A= MANE Select	NP_116759.2:p.His282=
NM_032976.4:c.753A=	NP_116758.1:p.Pro251=