Canonical Allele Identifier: CA1320966763

Gene: CASP10

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201208111G= , CM000664.2:g.201208111G=	GRCh38
NC_000002.11:g.202072834G= , CM000664.1:g.202072834G=	GRCh37
NC_000002.10:g.201781079G=	NCBI36
NG_007265.1:g.29980G= , LRG_33:g.29980G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313728.12:c.722-959G=	ENSP00000314599.7:n.722-959G=
ENST00000346817.10:c.721G=	ENSP00000237865.7:p.Gly241=
ENST00000438843.6:c.*307G=	ENSP00000401914.1:n.*307G=
ENST00000492363.6:c.758G=	ENSP00000512459.1:p.Arg253=
ENST00000696199.1:c.721+4345G=	ENSP00000512481.1:n.721+4345G=
ENST00000286186.11:c.850G= MANE Select	ENSP00000286186.6:p.Gly284=
ENST00000272879.9:c.850G=	ENSP00000272879.5:p.Gly284=
ENST00000286186.10:c.850G=	ENSP00000286186.6:p.Gly284=
ENST00000313728.11:c.722-959G=	ENSP00000314599.7:n.722-959G=
ENST00000346817.9:c.721G=	ENSP00000237865.7:p.Gly241=
ENST00000360132.7:c.758G=	ENSP00000353250.3:p.Arg253=
ENST00000438843.5:c.*307G=	ENSP00000401914.1:n.*307G=
ENST00000448480.1:c.721G=	ENSP00000396835.1:p.Gly241=
ENST00000492363.5:n.758G=
NM_001206524.1:c.722-959G=	NP_001193453.1:n.722-959G=
NM_001206542.1:c.721G=	NP_001193471.1:p.Gly241=
NM_001230.4:c.721G=	NP_001221.2:p.Gly241=
NM_032974.4:c.850G=	NP_116756.2:p.Gly284=
NM_032976.3:c.758G=	NP_116758.1:p.Arg253=
NM_032977.3:c.850G= , LRG_33t1:c.850G=	NP_116759.2:p.Gly284=
XM_005246907.2:c.847G=	XP_005246964.1:p.Gly283=
XM_006712796.2:c.100G=	XP_006712859.1:p.Gly34=
XM_011511990.1:c.755G=	XP_011510292.1:p.Arg252=
XR_923043.1:n.1054G=
XR_923044.1:n.962G=
XM_006712796.3:c.100G=	XP_006712859.1:p.Gly34=
XM_011511990.2:c.755G=	XP_011510292.1:p.Arg252=
XR_923043.2:n.1054G=
XR_923044.2:n.962G=
NM_001206524.2:c.722-959G=	NP_001193453.1:n.722-959G=
NM_001206542.2:c.721G=	NP_001193471.1:p.Gly241=
NM_001230.5:c.721G=	NP_001221.2:p.Gly241=
NM_032974.5:c.850G=	NP_116756.2:p.Gly284=
NM_032977.4:c.850G= MANE Select	NP_116759.2:p.Gly284=
NM_032976.4:c.758G=	NP_116758.1:p.Arg253=