Canonical Allele Identifier: CA1320966783

Gene: CASP10

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201208171C= , CM000664.2:g.201208171C=	GRCh38
NC_000002.11:g.202072894C= , CM000664.1:g.202072894C=	GRCh37
NC_000002.10:g.201781139C=	NCBI36
NG_007265.1:g.30040C= , LRG_33:g.30040C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313728.12:c.722-899C=	ENSP00000314599.7:n.722-899C=
ENST00000346817.10:c.781C=	ENSP00000237865.7:p.His261=
ENST00000438843.6:c.*367C=	ENSP00000401914.1:n.*367C=
ENST00000492363.6:c.818C=	ENSP00000512459.1:p.Pro273=
ENST00000696199.1:c.721+4405C=	ENSP00000512481.1:n.721+4405C=
ENST00000286186.11:c.910C= MANE Select	ENSP00000286186.6:p.His304=
ENST00000272879.9:c.910C=	ENSP00000272879.5:p.His304=
ENST00000286186.10:c.910C=	ENSP00000286186.6:p.His304=
ENST00000313728.11:c.722-899C=	ENSP00000314599.7:n.722-899C=
ENST00000346817.9:c.781C=	ENSP00000237865.7:p.His261=
ENST00000360132.7:c.818C=	ENSP00000353250.3:p.Pro273=
ENST00000448480.1:c.781C=	ENSP00000396835.1:p.His261=
ENST00000492363.5:n.818C=
NM_001206524.1:c.722-899C=	NP_001193453.1:n.722-899C=
NM_001206542.1:c.781C=	NP_001193471.1:p.His261=
NM_001230.4:c.781C=	NP_001221.2:p.His261=
NM_032974.4:c.910C=	NP_116756.2:p.His304=
NM_032976.3:c.818C=	NP_116758.1:p.Pro273=
NM_032977.3:c.910C= , LRG_33t1:c.910C=	NP_116759.2:p.His304=
XM_005246907.2:c.907C=	XP_005246964.1:p.His303=
XM_006712796.2:c.160C=	XP_006712859.1:p.His54=
XM_011511990.1:c.815C=	XP_011510292.1:p.Pro272=
XR_923043.1:n.1114C=
XR_923044.1:n.1022C=
XM_006712796.3:c.160C=	XP_006712859.1:p.His54=
XM_011511990.2:c.815C=	XP_011510292.1:p.Pro272=
XR_923043.2:n.1114C=
XR_923044.2:n.1022C=
NM_001206524.2:c.722-899C=	NP_001193453.1:n.722-899C=
NM_001206542.2:c.781C=	NP_001193471.1:p.His261=
NM_001230.5:c.781C=	NP_001221.2:p.His261=
NM_032974.5:c.910C=	NP_116756.2:p.His304=
NM_032977.4:c.910C= MANE Select	NP_116759.2:p.His304=
NM_032976.4:c.818C=	NP_116758.1:p.Pro273=