Canonical Allele Identifier: CA1519175643

Gene: CASP3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.184629422G= , CM000666.2:g.184629422G=	GRCh38
NC_000004.11:g.185550576G= , CM000666.1:g.185550576G=	GRCh37
NC_000004.10:g.185787570G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700100.1:c.684C=	ENSP00000514797.1:p.Asp228=
ENST00000700101.1:c.684C=	ENSP00000514798.1:p.Asp228=
ENST00000700102.1:n.2287C=
ENST00000700103.1:n.3649C=
ENST00000700104.1:c.*433C=	ENSP00000514799.1:n.*433C=
ENST00000308394.9:c.684C= MANE Select	ENSP00000311032.4:p.Asp228=
ENST00000308394.8:c.684C=	ENSP00000311032.4:p.Asp228=
ENST00000393585.6:c.*14C=	ENSP00000377210.2:n.*14C=
ENST00000393588.8:c.*14C=	ENSP00000377213.4:n.*14C=
ENST00000517513.5:c.*14C=	ENSP00000428372.1:n.*14C=
ENST00000523916.5:c.684C=	ENSP00000428929.1:p.Asp228=
ENST00000613118.4:c.*117C=	ENSP00000478339.1:n.*117C=
NM_004346.3:c.684C=	NP_004337.2:p.Asp228=
NM_032991.2:c.684C=	NP_116786.1:p.Asp228=
XM_011532301.1:c.684C=	XP_011530603.1:p.Asp228=
NM_001354777.1:c.684C=	NP_001341706.1:p.Asp228=
NM_001354779.1:c.606C=	NP_001341708.1:p.Asp202=
NM_001354780.1:c.606C=	NP_001341709.1:p.Asp202=
NM_001354781.1:c.*14C=	NP_001341710.1:n.*14C=
NM_001354782.1:c.*14C=	NP_001341711.1:n.*14C=
NM_001354783.1:c.*14C=	NP_001341712.1:n.*14C=
NM_001354784.1:c.*14C=	NP_001341713.1:n.*14C=
NM_004346.4:c.684C= MANE Select	NP_004337.2:p.Asp228=
NM_001354777.2:c.684C=	NP_001341706.1:p.Asp228=
NM_001354779.2:c.606C=	NP_001341708.1:p.Asp202=
NM_001354780.2:c.606C=	NP_001341709.1:p.Asp202=
NM_001354781.2:c.*14C=	NP_001341710.1:n.*14C=
NM_001354782.2:c.*14C=	NP_001341711.1:n.*14C=
NM_001354783.2:c.*14C=	NP_001341712.1:n.*14C=
NM_001354784.2:c.*14C=	NP_001341713.1:n.*14C=
NM_032991.3:c.684C=	NP_116786.1:p.Asp228=