Canonical Allele Identifier: CA1519175083

Gene: CASP3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.184629003A= , CM000666.2:g.184629003A=	GRCh38
NC_000004.11:g.185550157A= , CM000666.1:g.185550157A=	GRCh37
NC_000004.10:g.185787151A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700100.1:c.*269T=	ENSP00000514797.1:n.*269T=
ENST00000700101.1:c.*269T=	ENSP00000514798.1:n.*269T=
ENST00000700102.1:n.2706T=
ENST00000700103.1:n.4068T=
ENST00000700104.1:c.*852T=	ENSP00000514799.1:n.*852T=
ENST00000308394.9:c.*269T= MANE Select	ENSP00000311032.4:n.*269T=
ENST00000308394.8:c.*269T=	ENSP00000311032.4:n.*269T=
ENST00000393585.6:c.*433T=	ENSP00000377210.2:n.*433T=
ENST00000523916.5:c.*269T=	ENSP00000428929.1:n.*269T=
ENST00000613118.4:c.*536T=	ENSP00000478339.1:n.*536T=
NM_004346.3:c.*269T=	NP_004337.2:n.*269T=
NM_032991.2:c.*269T=	NP_116786.1:n.*269T=
XM_011532301.1:c.*269T=	XP_011530603.1:n.*269T=
NM_001354777.1:c.*269T=	NP_001341706.1:n.*269T=
NM_001354779.1:c.*269T=	NP_001341708.1:n.*269T=
NM_001354780.1:c.*269T=	NP_001341709.1:n.*269T=
NM_001354781.1:c.*433T=	NP_001341710.1:n.*433T=
NM_001354782.1:c.*433T=	NP_001341711.1:n.*433T=
NM_001354783.1:c.*433T=	NP_001341712.1:n.*433T=
NM_001354784.1:c.*433T=	NP_001341713.1:n.*433T=
NM_004346.4:c.*269T= MANE Select	NP_004337.2:n.*269T=
NM_001354777.2:c.*269T=	NP_001341706.1:n.*269T=
NM_001354779.2:c.*269T=	NP_001341708.1:n.*269T=
NM_001354780.2:c.*269T=	NP_001341709.1:n.*269T=
NM_001354781.2:c.*433T=	NP_001341710.1:n.*433T=
NM_001354782.2:c.*433T=	NP_001341711.1:n.*433T=
NM_001354783.2:c.*433T=	NP_001341712.1:n.*433T=
NM_001354784.2:c.*433T=	NP_001341713.1:n.*433T=
NM_032991.3:c.*269T=	NP_116786.1:n.*269T=