Canonical Allele Identifier: CA1320966777

Gene: CASP10

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201208145C= , CM000664.2:g.201208145C=	GRCh38
NC_000002.11:g.202072868C= , CM000664.1:g.202072868C=	GRCh37
NC_000002.10:g.201781113C=	NCBI36
NG_007265.1:g.30014C= , LRG_33:g.30014C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313728.12:c.722-925C=	ENSP00000314599.7:n.722-925C=
ENST00000346817.10:c.755C=	ENSP00000237865.7:p.Thr252=
ENST00000438843.6:c.*341C=	ENSP00000401914.1:n.*341C=
ENST00000492363.6:c.792C=	ENSP00000512459.1:p.Tyr264=
ENST00000696199.1:c.721+4379C=	ENSP00000512481.1:n.721+4379C=
ENST00000286186.11:c.884C= MANE Select	ENSP00000286186.6:p.Thr295=
ENST00000272879.9:c.884C=	ENSP00000272879.5:p.Thr295=
ENST00000286186.10:c.884C=	ENSP00000286186.6:p.Thr295=
ENST00000313728.11:c.722-925C=	ENSP00000314599.7:n.722-925C=
ENST00000346817.9:c.755C=	ENSP00000237865.7:p.Thr252=
ENST00000360132.7:c.792C=	ENSP00000353250.3:p.Tyr264=
ENST00000438843.5:c.*341C=	ENSP00000401914.1:n.*341C=
ENST00000448480.1:c.755C=	ENSP00000396835.1:p.Thr252=
ENST00000492363.5:n.792C=
NM_001206524.1:c.722-925C=	NP_001193453.1:n.722-925C=
NM_001206542.1:c.755C=	NP_001193471.1:p.Thr252=
NM_001230.4:c.755C=	NP_001221.2:p.Thr252=
NM_032974.4:c.884C=	NP_116756.2:p.Thr295=
NM_032976.3:c.792C=	NP_116758.1:p.Tyr264=
NM_032977.3:c.884C= , LRG_33t1:c.884C=	NP_116759.2:p.Thr295=
XM_005246907.2:c.881C=	XP_005246964.1:p.Thr294=
XM_006712796.2:c.134C=	XP_006712859.1:p.Thr45=
XM_011511990.1:c.789C=	XP_011510292.1:p.Tyr263=
XR_923043.1:n.1088C=
XR_923044.1:n.996C=
XM_006712796.3:c.134C=	XP_006712859.1:p.Thr45=
XM_011511990.2:c.789C=	XP_011510292.1:p.Tyr263=
XR_923043.2:n.1088C=
XR_923044.2:n.996C=
NM_001206524.2:c.722-925C=	NP_001193453.1:n.722-925C=
NM_001206542.2:c.755C=	NP_001193471.1:p.Thr252=
NM_001230.5:c.755C=	NP_001221.2:p.Thr252=
NM_032974.5:c.884C=	NP_116756.2:p.Thr295=
NM_032977.4:c.884C= MANE Select	NP_116759.2:p.Thr295=
NM_032976.4:c.792C=	NP_116758.1:p.Tyr264=