Canonical Allele Identifier: CA1519162710

Gene: CASP3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.184649240C= , CM000666.2:g.184649240C=	GRCh38
NC_000004.11:g.185570394C= , CM000666.1:g.185570394C=	GRCh37
NC_000004.10:g.185807388C=	NCBI36
NG_051582.1:g.4628C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000700101.1:c.-16+752G=	ENSP00000514798.1:n.-16+752G=
ENST00000700102.1:n.53+155G=
ENST00000700103.1:n.53+155G=
ENST00000700104.1:c.-16+155G=	ENSP00000514799.1:n.-16+155G=
ENST00000308394.9:c.-183+155G= MANE Select	ENSP00000311032.4:n.-183+155G=
ENST00000308394.8:c.-183+155G=	ENSP00000311032.4:n.-183+155G=
ENST00000393588.8:c.-16+155G=	ENSP00000377213.4:n.-16+155G=
ENST00000447121.2:c.-145+155G=	ENSP00000407142.2:n.-145+155G=
ENST00000517513.5:c.-183+155G=	ENSP00000428372.1:n.-183+155G=
ENST00000523916.5:c.-16+155G=	ENSP00000428929.1:n.-16+155G=
NM_004346.3:c.-183+155G=	NP_004337.2:n.-183+155G=
NM_032991.2:c.-16+155G=	NP_116786.1:n.-16+155G=
XM_011532301.1:c.-145+155G=	XP_011530603.1:n.-145+155G=
NM_001354777.1:c.-145+155G=	NP_001341706.1:n.-145+155G=
NM_001354779.1:c.-90+155G=	NP_001341708.1:n.-90+155G=
NM_001354780.1:c.-257+155G=	NP_001341709.1:n.-257+155G=
NM_001354781.1:c.-16+155G=	NP_001341710.1:n.-16+155G=
NM_001354782.1:c.-183+155G=	NP_001341711.1:n.-183+155G=
NM_001354783.1:c.-348+155G=	NP_001341712.1:n.-348+155G=
NM_001354784.1:c.-90+155G=	NP_001341713.1:n.-90+155G=
NM_004346.4:c.-183+155G= MANE Select	NP_004337.2:n.-183+155G=
NM_001354777.2:c.-145+155G=	NP_001341706.1:n.-145+155G=
NM_001354779.2:c.-90+155G=	NP_001341708.1:n.-90+155G=
NM_001354780.2:c.-257+155G=	NP_001341709.1:n.-257+155G=
NM_001354781.2:c.-16+155G=	NP_001341710.1:n.-16+155G=
NM_001354782.2:c.-183+155G=	NP_001341711.1:n.-183+155G=
NM_001354783.2:c.-348+155G=	NP_001341712.1:n.-348+155G=
NM_001354784.2:c.-90+155G=	NP_001341713.1:n.-90+155G=
NM_032991.3:c.-16+155G=	NP_116786.1:n.-16+155G=