Canonical Allele Identifier: CA1320966756

Gene: CASP10

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201208094T= , CM000664.2:g.201208094T=	GRCh38
NC_000002.11:g.202072817T= , CM000664.1:g.202072817T=	GRCh37
NC_000002.10:g.201781062T=	NCBI36
NG_007265.1:g.29963T= , LRG_33:g.29963T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313728.12:c.722-976T=	ENSP00000314599.7:n.722-976T=
ENST00000346817.10:c.704T=	ENSP00000237865.7:p.Met235=
ENST00000438843.6:c.*290T=	ENSP00000401914.1:n.*290T=
ENST00000492363.6:c.741T=	ENSP00000512459.1:p.Asp247=
ENST00000696199.1:c.721+4328T=	ENSP00000512481.1:n.721+4328T=
ENST00000286186.11:c.833T= MANE Select	ENSP00000286186.6:p.Met278=
ENST00000272879.9:c.833T=	ENSP00000272879.5:p.Met278=
ENST00000286186.10:c.833T=	ENSP00000286186.6:p.Met278=
ENST00000313728.11:c.722-976T=	ENSP00000314599.7:n.722-976T=
ENST00000346817.9:c.704T=	ENSP00000237865.7:p.Met235=
ENST00000360132.7:c.741T=	ENSP00000353250.3:p.Asp247=
ENST00000438843.5:c.*290T=	ENSP00000401914.1:n.*290T=
ENST00000448480.1:c.704T=	ENSP00000396835.1:p.Met235=
ENST00000492363.5:n.741T=
NM_001206524.1:c.722-976T=	NP_001193453.1:n.722-976T=
NM_001206542.1:c.704T=	NP_001193471.1:p.Met235=
NM_001230.4:c.704T=	NP_001221.2:p.Met235=
NM_032974.4:c.833T=	NP_116756.2:p.Met278=
NM_032976.3:c.741T=	NP_116758.1:p.Asp247=
NM_032977.3:c.833T= , LRG_33t1:c.833T=	NP_116759.2:p.Met278=
XM_005246907.2:c.830T=	XP_005246964.1:p.Met277=
XM_006712796.2:c.83T=	XP_006712859.1:p.Met28=
XM_011511990.1:c.738T=	XP_011510292.1:p.Asp246=
XR_923043.1:n.1037T=
XR_923044.1:n.945T=
XM_006712796.3:c.83T=	XP_006712859.1:p.Met28=
XM_011511990.2:c.738T=	XP_011510292.1:p.Asp246=
XR_923043.2:n.1037T=
XR_923044.2:n.945T=
NM_001206524.2:c.722-976T=	NP_001193453.1:n.722-976T=
NM_001206542.2:c.704T=	NP_001193471.1:p.Met235=
NM_001230.5:c.704T=	NP_001221.2:p.Met235=
NM_032974.5:c.833T=	NP_116756.2:p.Met278=
NM_032977.4:c.833T= MANE Select	NP_116759.2:p.Met278=
NM_032976.4:c.741T=	NP_116758.1:p.Asp247=