Canonical Allele Identifier: CA2764832350

Gene: CASP3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.184649342del , CM000666.2:g.184649342del	GRCh38
NC_000004.11:g.185570496del , CM000666.1:g.185570496del	GRCh37
NC_000004.10:g.185807490del	NCBI36
NG_051582.1:g.4730del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700101.1:c.-16+650del	ENSP00000514798.1:n.-16+650del
ENST00000700102.1:n.53+53del
ENST00000700103.1:n.53+53del
ENST00000700104.1:c.-16+53del	ENSP00000514799.1:n.-16+53del
ENST00000308394.9:c.-183+53del MANE Select	ENSP00000311032.4:n.-183+53del
ENST00000308394.8:c.-183+53del	ENSP00000311032.4:n.-183+53del
ENST00000393588.8:c.-16+53del	ENSP00000377213.4:n.-16+53del
ENST00000447121.2:c.-145+53del	ENSP00000407142.2:n.-145+53del
ENST00000517513.5:c.-183+53del	ENSP00000428372.1:n.-183+53del
ENST00000523916.5:c.-16+53del	ENSP00000428929.1:n.-16+53del
NM_004346.3:c.-183+53del	NP_004337.2:n.-183+53del
NM_032991.2:c.-16+53del	NP_116786.1:n.-16+53del
XM_011532301.1:c.-145+53del	XP_011530603.1:n.-145+53del
NM_001354777.1:c.-145+53del	NP_001341706.1:n.-145+53del
NM_001354779.1:c.-90+53del	NP_001341708.1:n.-90+53del
NM_001354780.1:c.-257+53del	NP_001341709.1:n.-257+53del
NM_001354781.1:c.-16+53del	NP_001341710.1:n.-16+53del
NM_001354782.1:c.-183+53del	NP_001341711.1:n.-183+53del
NM_001354783.1:c.-348+53del	NP_001341712.1:n.-348+53del
NM_001354784.1:c.-90+53del	NP_001341713.1:n.-90+53del
NM_004346.4:c.-183+53del MANE Select	NP_004337.2:n.-183+53del
NM_001354777.2:c.-145+53del	NP_001341706.1:n.-145+53del
NM_001354779.2:c.-90+53del	NP_001341708.1:n.-90+53del
NM_001354780.2:c.-257+53del	NP_001341709.1:n.-257+53del
NM_001354781.2:c.-16+53del	NP_001341710.1:n.-16+53del
NM_001354782.2:c.-183+53del	NP_001341711.1:n.-183+53del
NM_001354783.2:c.-348+53del	NP_001341712.1:n.-348+53del
NM_001354784.2:c.-90+53del	NP_001341713.1:n.-90+53del
NM_032991.3:c.-16+53del	NP_116786.1:n.-16+53del