Canonical Allele Identifier: CA1320966787

Gene: CASP10

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201208180G= , CM000664.2:g.201208180G=	GRCh38
NC_000002.11:g.202072903G= , CM000664.1:g.202072903G=	GRCh37
NC_000002.10:g.201781148G=	NCBI36
NG_007265.1:g.30049G= , LRG_33:g.30049G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313728.12:c.722-890G=	ENSP00000314599.7:n.722-890G=
ENST00000346817.10:c.790G=	ENSP00000237865.7:p.Ala264=
ENST00000438843.6:c.*376G=	ENSP00000401914.1:n.*376G=
ENST00000492363.6:c.*5G=	ENSP00000512459.1:n.*5G=
ENST00000696199.1:c.721+4414G=	ENSP00000512481.1:n.721+4414G=
ENST00000286186.11:c.919G= MANE Select	ENSP00000286186.6:p.Ala307=
ENST00000272879.9:c.919G=	ENSP00000272879.5:p.Ala307=
ENST00000286186.10:c.919G=	ENSP00000286186.6:p.Ala307=
ENST00000313728.11:c.722-890G=	ENSP00000314599.7:n.722-890G=
ENST00000346817.9:c.790G=	ENSP00000237865.7:p.Ala264=
ENST00000360132.7:c.*5G=	ENSP00000353250.3:n.*5G=
ENST00000448480.1:c.790G=	ENSP00000396835.1:p.Ala264=
ENST00000492363.5:n.827G=
NM_001206524.1:c.722-890G=	NP_001193453.1:n.722-890G=
NM_001206542.1:c.790G=	NP_001193471.1:p.Ala264=
NM_001230.4:c.790G=	NP_001221.2:p.Ala264=
NM_032974.4:c.919G=	NP_116756.2:p.Ala307=
NM_032976.3:c.*5G=	NP_116758.1:n.*5G=
NM_032977.3:c.919G= , LRG_33t1:c.919G=	NP_116759.2:p.Ala307=
XM_005246907.2:c.916G=	XP_005246964.1:p.Ala306=
XM_006712796.2:c.169G=	XP_006712859.1:p.Ala57=
XM_011511990.1:c.*5G=	XP_011510292.1:n.*5G=
XR_923043.1:n.1123G=
XR_923044.1:n.1031G=
XM_006712796.3:c.169G=	XP_006712859.1:p.Ala57=
XM_011511990.2:c.*5G=	XP_011510292.1:n.*5G=
XR_923043.2:n.1123G=
XR_923044.2:n.1031G=
NM_001206524.2:c.722-890G=	NP_001193453.1:n.722-890G=
NM_001206542.2:c.790G=	NP_001193471.1:p.Ala264=
NM_001230.5:c.790G=	NP_001221.2:p.Ala264=
NM_032974.5:c.919G=	NP_116756.2:p.Ala307=
NM_032977.4:c.919G= MANE Select	NP_116759.2:p.Ala307=
NM_032976.4:c.*5G=	NP_116758.1:n.*5G=