Canonical Allele Identifier: CA1320966732

Gene: CASP10

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201208047T= , CM000664.2:g.201208047T=	GRCh38
NC_000002.11:g.202072770T= , CM000664.1:g.202072770T=	GRCh37
NC_000002.10:g.201781015T=	NCBI36
NG_007265.1:g.29916T= , LRG_33:g.29916T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313728.12:c.722-1023T=	ENSP00000314599.7:n.722-1023T=
ENST00000346817.10:c.685-28T=	ENSP00000237865.7:n.685-28T=
ENST00000438843.6:c.*271-28T=	ENSP00000401914.1:n.*271-28T=
ENST00000492363.6:c.722-28T=	ENSP00000512459.1:n.722-28T=
ENST00000696199.1:c.721+4281T=	ENSP00000512481.1:n.721+4281T=
ENST00000286186.11:c.814-28T= MANE Select	ENSP00000286186.6:n.814-28T=
ENST00000272879.9:c.814-28T=	ENSP00000272879.5:n.814-28T=
ENST00000286186.10:c.814-28T=	ENSP00000286186.6:n.814-28T=
ENST00000313728.11:c.722-1023T=	ENSP00000314599.7:n.722-1023T=
ENST00000346817.9:c.685-28T=	ENSP00000237865.7:n.685-28T=
ENST00000360132.7:c.722-28T=	ENSP00000353250.3:n.722-28T=
ENST00000438843.5:c.*271-28T=	ENSP00000401914.1:n.*271-28T=
ENST00000448480.1:c.685-28T=	ENSP00000396835.1:n.685-28T=
ENST00000492363.5:n.722-28T=
NM_001206524.1:c.722-1023T=	NP_001193453.1:n.722-1023T=
NM_001206542.1:c.685-28T=	NP_001193471.1:n.685-28T=
NM_001230.4:c.685-28T=	NP_001221.2:n.685-28T=
NM_032974.4:c.814-28T=	NP_116756.2:n.814-28T=
NM_032976.3:c.722-28T=	NP_116758.1:n.722-28T=
NM_032977.3:c.814-28T= , LRG_33t1:c.814-28T=	NP_116759.2:n.814-28T=
XM_005246907.2:c.811-28T=	XP_005246964.1:n.811-28T=
XM_006712796.2:c.64-28T=	XP_006712859.1:n.64-28T=
XM_011511990.1:c.719-28T=	XP_011510292.1:n.719-28T=
XR_923043.1:n.1018-28T=
XR_923044.1:n.926-28T=
XM_006712796.3:c.64-28T=	XP_006712859.1:n.64-28T=
XM_011511990.2:c.719-28T=	XP_011510292.1:n.719-28T=
XR_923043.2:n.1018-28T=
XR_923044.2:n.926-28T=
NM_001206524.2:c.722-1023T=	NP_001193453.1:n.722-1023T=
NM_001206542.2:c.685-28T=	NP_001193471.1:n.685-28T=
NM_001230.5:c.685-28T=	NP_001221.2:n.685-28T=
NM_032974.5:c.814-28T=	NP_116756.2:n.814-28T=
NM_032977.4:c.814-28T= MANE Select	NP_116759.2:n.814-28T=
NM_032976.4:c.722-28T=	NP_116758.1:n.722-28T=