Canonical Allele Identifier: CA1320967385

Gene: CASP10

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201209460T= , CM000664.2:g.201209460T=	GRCh38
NC_000002.11:g.202074183T= , CM000664.1:g.202074183T=	GRCh37
NC_000002.10:g.201782428T=	NCBI36
NG_007265.1:g.31329T= , LRG_33:g.31329T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313728.12:c.1112T=	ENSP00000314599.7:p.Leu371=
ENST00000346817.10:c.1184T=	ENSP00000237865.7:p.Leu395=
ENST00000438843.6:c.*770T=	ENSP00000401914.1:n.*770T=
ENST00000492363.6:c.*399T=	ENSP00000512459.1:n.*399T=
ENST00000696199.1:c.721+5694T=	ENSP00000512481.1:n.721+5694T=
ENST00000286186.11:c.1313T= MANE Select	ENSP00000286186.6:p.Leu438=
ENST00000272879.9:c.1313T=	ENSP00000272879.5:p.Leu438=
ENST00000286186.10:c.1313T=	ENSP00000286186.6:p.Leu438=
ENST00000313728.11:c.1112T=	ENSP00000314599.7:p.Leu371=
ENST00000346817.9:c.1184T=	ENSP00000237865.7:p.Leu395=
ENST00000360132.7:c.*399T=	ENSP00000353250.3:n.*399T=
ENST00000448480.1:c.1184T=	ENSP00000396835.1:p.Leu395=
ENST00000492363.5:n.1221T=
NM_001206524.1:c.1112T=	NP_001193453.1:p.Leu371=
NM_001206542.1:c.1184T=	NP_001193471.1:p.Leu395=
NM_001230.4:c.1184T=	NP_001221.2:p.Leu395=
NM_032974.4:c.1313T=	NP_116756.2:p.Leu438=
NM_032976.3:c.*399T=	NP_116758.1:n.*399T=
NM_032977.3:c.1313T= , LRG_33t1:c.1313T=	NP_116759.2:p.Leu438=
XM_005246907.2:c.1310T=	XP_005246964.1:p.Leu437=
XM_006712796.2:c.563T=	XP_006712859.1:p.Leu188=
XM_006712796.3:c.563T=	XP_006712859.1:p.Leu188=
NM_001206524.2:c.1112T=	NP_001193453.1:p.Leu371=
NM_001206542.2:c.1184T=	NP_001193471.1:p.Leu395=
NM_001230.5:c.1184T=	NP_001221.2:p.Leu395=
NM_032974.5:c.1313T=	NP_116756.2:p.Leu438=
NM_032977.4:c.1313T= MANE Select	NP_116759.2:p.Leu438=
NM_032976.4:c.*399T=	NP_116758.1:n.*399T=