Canonical Allele Identifier: CA1519162415

Gene: CASP3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.184649019_184649020delinsCT , CM000666.2:g.184649019_184649020delinsCT	GRCh38
NC_000004.11:g.185570173_185570174delinsCT , CM000666.1:g.185570173_185570174delinsCT	GRCh37
NC_000004.10:g.185807167_185807168delinsCT	NCBI36
NG_051582.1:g.4407_4408delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700101.1:c.-16+972_-16+973delinsAG	ENSP00000514798.1:n.-16+972_-16+973delinsAG
ENST00000700102.1:n.53+375_53+376delinsAG
ENST00000700103.1:n.53+375_53+376delinsAG
ENST00000700104.1:c.-16+375_-16+376delinsAG	ENSP00000514799.1:n.-16+375_-16+376delinsAG
ENST00000308394.9:c.-183+375_-183+376delinsAG MANE Select	ENSP00000311032.4:n.-183+375_-183+376delinsAG
ENST00000308394.8:c.-183+375_-183+376delinsAG	ENSP00000311032.4:n.-183+375_-183+376delinsAG
ENST00000393588.8:c.-16+375_-16+376delinsAG	ENSP00000377213.4:n.-16+375_-16+376delinsAG
ENST00000447121.2:c.-145+375_-145+376delinsAG	ENSP00000407142.2:n.-145+375_-145+376delinsAG
ENST00000517513.5:c.-183+375_-183+376delinsAG	ENSP00000428372.1:n.-183+375_-183+376delinsAG
ENST00000523916.5:c.-16+375_-16+376delinsAG	ENSP00000428929.1:n.-16+375_-16+376delinsAG
NM_004346.3:c.-183+375_-183+376delinsAG	NP_004337.2:n.-183+375_-183+376delinsAG
NM_032991.2:c.-16+375_-16+376delinsAG	NP_116786.1:n.-16+375_-16+376delinsAG
XM_011532301.1:c.-145+375_-145+376delinsAG	XP_011530603.1:n.-145+375_-145+376delinsAG
NM_001354777.1:c.-145+375_-145+376delinsAG	NP_001341706.1:n.-145+375_-145+376delinsAG
NM_001354779.1:c.-90+375_-90+376delinsAG	NP_001341708.1:n.-90+375_-90+376delinsAG
NM_001354780.1:c.-257+375_-257+376delinsAG	NP_001341709.1:n.-257+375_-257+376delinsAG
NM_001354781.1:c.-16+375_-16+376delinsAG	NP_001341710.1:n.-16+375_-16+376delinsAG
NM_001354782.1:c.-183+375_-183+376delinsAG	NP_001341711.1:n.-183+375_-183+376delinsAG
NM_001354783.1:c.-348+375_-348+376delinsAG	NP_001341712.1:n.-348+375_-348+376delinsAG
NM_001354784.1:c.-90+375_-90+376delinsAG	NP_001341713.1:n.-90+375_-90+376delinsAG
NM_004346.4:c.-183+375_-183+376delinsAG MANE Select	NP_004337.2:n.-183+375_-183+376delinsAG
NM_001354777.2:c.-145+375_-145+376delinsAG	NP_001341706.1:n.-145+375_-145+376delinsAG
NM_001354779.2:c.-90+375_-90+376delinsAG	NP_001341708.1:n.-90+375_-90+376delinsAG
NM_001354780.2:c.-257+375_-257+376delinsAG	NP_001341709.1:n.-257+375_-257+376delinsAG
NM_001354781.2:c.-16+375_-16+376delinsAG	NP_001341710.1:n.-16+375_-16+376delinsAG
NM_001354782.2:c.-183+375_-183+376delinsAG	NP_001341711.1:n.-183+375_-183+376delinsAG
NM_001354783.2:c.-348+375_-348+376delinsAG	NP_001341712.1:n.-348+375_-348+376delinsAG
NM_001354784.2:c.-90+375_-90+376delinsAG	NP_001341713.1:n.-90+375_-90+376delinsAG
NM_032991.3:c.-16+375_-16+376delinsAG	NP_116786.1:n.-16+375_-16+376delinsAG