Canonical Allele Identifier: CA1320967392

Gene: CASP10

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201209476C= , CM000664.2:g.201209476C=	GRCh38
NC_000002.11:g.202074199C= , CM000664.1:g.202074199C=	GRCh37
NC_000002.10:g.201782444C=	NCBI36
NG_007265.1:g.31345C= , LRG_33:g.31345C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313728.12:c.1128C=	ENSP00000314599.7:p.Val376=
ENST00000346817.10:c.1200C=	ENSP00000237865.7:p.Val400=
ENST00000438843.6:c.*786C=	ENSP00000401914.1:n.*786C=
ENST00000492363.6:c.*415C=	ENSP00000512459.1:n.*415C=
ENST00000696199.1:c.721+5710C=	ENSP00000512481.1:n.721+5710C=
ENST00000286186.11:c.1329C= MANE Select	ENSP00000286186.6:p.Val443=
ENST00000272879.9:c.1329C=	ENSP00000272879.5:p.Val443=
ENST00000286186.10:c.1329C=	ENSP00000286186.6:p.Val443=
ENST00000313728.11:c.1128C=	ENSP00000314599.7:p.Val376=
ENST00000346817.9:c.1200C=	ENSP00000237865.7:p.Val400=
ENST00000360132.7:c.*415C=	ENSP00000353250.3:n.*415C=
ENST00000448480.1:c.1200C=	ENSP00000396835.1:p.Val400=
ENST00000492363.5:n.1237C=
NM_001206524.1:c.1128C=	NP_001193453.1:p.Val376=
NM_001206542.1:c.1200C=	NP_001193471.1:p.Val400=
NM_001230.4:c.1200C=	NP_001221.2:p.Val400=
NM_032974.4:c.1329C=	NP_116756.2:p.Val443=
NM_032976.3:c.*415C=	NP_116758.1:n.*415C=
NM_032977.3:c.1329C= , LRG_33t1:c.1329C=	NP_116759.2:p.Val443=
XM_005246907.2:c.1326C=	XP_005246964.1:p.Val442=
XM_006712796.2:c.579C=	XP_006712859.1:p.Val193=
XM_006712796.3:c.579C=	XP_006712859.1:p.Val193=
NM_001206524.2:c.1128C=	NP_001193453.1:p.Val376=
NM_001206542.2:c.1200C=	NP_001193471.1:p.Val400=
NM_001230.5:c.1200C=	NP_001221.2:p.Val400=
NM_032974.5:c.1329C=	NP_116756.2:p.Val443=
NM_032977.4:c.1329C= MANE Select	NP_116759.2:p.Val443=
NM_032976.4:c.*415C=	NP_116758.1:n.*415C=