Canonical Allele Identifier: CA1320966790

Gene: CASP10

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201208184G= , CM000664.2:g.201208184G=	GRCh38
NC_000002.11:g.202072907G= , CM000664.1:g.202072907G=	GRCh37
NC_000002.10:g.201781152G=	NCBI36
NG_007265.1:g.30053G= , LRG_33:g.30053G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313728.12:c.722-886G=	ENSP00000314599.7:n.722-886G=
ENST00000346817.10:c.793+1G=	ENSP00000237865.7:n.793+1G=
ENST00000438843.6:c.*379+1G=	ENSP00000401914.1:n.*379+1G=
ENST00000492363.6:c.*8+1G=	ENSP00000512459.1:n.*8+1G=
ENST00000696199.1:c.721+4418G=	ENSP00000512481.1:n.721+4418G=
ENST00000286186.11:c.922+1G= MANE Select	ENSP00000286186.6:n.922+1G=
ENST00000272879.9:c.922+1G=	ENSP00000272879.5:n.922+1G=
ENST00000286186.10:c.922+1G=	ENSP00000286186.6:n.922+1G=
ENST00000313728.11:c.722-886G=	ENSP00000314599.7:n.722-886G=
ENST00000346817.9:c.793+1G=	ENSP00000237865.7:n.793+1G=
ENST00000360132.7:c.*8+1G=	ENSP00000353250.3:n.*8+1G=
ENST00000448480.1:c.793+1G=	ENSP00000396835.1:n.793+1G=
ENST00000492363.5:n.830+1G=
NM_001206524.1:c.722-886G=	NP_001193453.1:n.722-886G=
NM_001206542.1:c.793+1G=	NP_001193471.1:n.793+1G=
NM_001230.4:c.793+1G=	NP_001221.2:n.793+1G=
NM_032974.4:c.922+1G=	NP_116756.2:n.922+1G=
NM_032976.3:c.*8+1G=	NP_116758.1:n.*8+1G=
NM_032977.3:c.922+1G= , LRG_33t1:c.922+1G=	NP_116759.2:n.922+1G=
XM_005246907.2:c.919+1G=	XP_005246964.1:n.919+1G=
XM_006712796.2:c.172+1G=	XP_006712859.1:n.172+1G=
XM_011511990.1:c.*8+1G=	XP_011510292.1:n.*8+1G=
XR_923043.1:n.1126+1G=
XR_923044.1:n.1034+1G=
XM_006712796.3:c.172+1G=	XP_006712859.1:n.172+1G=
XM_011511990.2:c.*8+1G=	XP_011510292.1:n.*8+1G=
XR_923043.2:n.1126+1G=
XR_923044.2:n.1034+1G=
NM_001206524.2:c.722-886G=	NP_001193453.1:n.722-886G=
NM_001206542.2:c.793+1G=	NP_001193471.1:n.793+1G=
NM_001230.5:c.793+1G=	NP_001221.2:n.793+1G=
NM_032974.5:c.922+1G=	NP_116756.2:n.922+1G=
NM_032977.4:c.922+1G= MANE Select	NP_116759.2:n.922+1G=
NM_032976.4:c.*8+1G=	NP_116758.1:n.*8+1G=