Canonical Allele Identifier: CA1519161763

Gene: CASP3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.184648518C= , CM000666.2:g.184648518C=	GRCh38
NC_000004.11:g.185569672C= , CM000666.1:g.185569672C=	GRCh37
NC_000004.10:g.185806666C=	NCBI36
NG_051582.1:g.3906C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700100.1:c.-69G=	ENSP00000514797.1:n.-69G=
ENST00000700101.1:c.-16+1474G=	ENSP00000514798.1:n.-16+1474G=
ENST00000700102.1:n.53+877G=
ENST00000700103.1:n.53+877G=
ENST00000700104.1:c.-16+877G=	ENSP00000514799.1:n.-16+877G=
ENST00000308394.9:c.-69G= MANE Select	ENSP00000311032.4:n.-69G=
ENST00000308394.8:c.-69G=	ENSP00000311032.4:n.-69G=
ENST00000393585.6:c.-261G=	ENSP00000377210.2:n.-261G=
ENST00000393588.8:c.-16+877G=	ENSP00000377213.4:n.-16+877G=
ENST00000447121.2:c.-31G=	ENSP00000407142.2:n.-31G=
ENST00000517513.5:c.-69G=	ENSP00000428372.1:n.-69G=
ENST00000523916.5:c.-16+877G=	ENSP00000428929.1:n.-16+877G=
ENST00000613118.4:c.-234G=	ENSP00000478339.1:n.-234G=
NM_004346.3:c.-69G=	NP_004337.2:n.-69G=
NM_032991.2:c.-16+877G=	NP_116786.1:n.-16+877G=
XM_011532301.1:c.-31G=	XP_011530603.1:n.-31G=
NM_001354777.1:c.-31G=	NP_001341706.1:n.-31G=
NM_001354779.1:c.-90+877G=	NP_001341708.1:n.-90+877G=
NM_001354780.1:c.-143G=	NP_001341709.1:n.-143G=
NM_001354781.1:c.-16+877G=	NP_001341710.1:n.-16+877G=
NM_001354782.1:c.-69G=	NP_001341711.1:n.-69G=
NM_001354783.1:c.-234G=	NP_001341712.1:n.-234G=
NM_001354784.1:c.-90+877G=	NP_001341713.1:n.-90+877G=
NM_004346.4:c.-69G= MANE Select	NP_004337.2:n.-69G=
NM_001354777.2:c.-31G=	NP_001341706.1:n.-31G=
NM_001354779.2:c.-90+877G=	NP_001341708.1:n.-90+877G=
NM_001354780.2:c.-143G=	NP_001341709.1:n.-143G=
NM_001354781.2:c.-16+877G=	NP_001341710.1:n.-16+877G=
NM_001354782.2:c.-69G=	NP_001341711.1:n.-69G=
NM_001354783.2:c.-234G=	NP_001341712.1:n.-234G=
NM_001354784.2:c.-90+877G=	NP_001341713.1:n.-90+877G=
NM_032991.3:c.-16+877G=	NP_116786.1:n.-16+877G=