Canonical Allele Identifier: CA1519161280

Gene: CASP3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.184648096_184648097delinsAC , CM000666.2:g.184648096_184648097delinsAC	GRCh38
NC_000004.11:g.185569250_185569251delinsAC , CM000666.1:g.185569250_185569251delinsAC	GRCh37
NC_000004.10:g.185806244_185806245delinsAC	NCBI36
NG_051582.1:g.3484_3485delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700100.1:c.-16+368_-16+369delinsGT	ENSP00000514797.1:n.-16+368_-16+369delinsGT
ENST00000700101.1:c.-16+1895_-16+1896delinsGT	ENSP00000514798.1:n.-16+1895_-16+1896delinsGT
ENST00000700102.1:n.53+1298_53+1299delinsGT
ENST00000700103.1:n.53+1298_53+1299delinsGT
ENST00000700104.1:c.-16+1298_-16+1299delinsGT	ENSP00000514799.1:n.-16+1298_-16+1299delinsGT
ENST00000308394.9:c.-16+368_-16+369delinsGT MANE Select	ENSP00000311032.4:n.-16+368_-16+369delinsGT
ENST00000308394.8:c.-16+368_-16+369delinsGT	ENSP00000311032.4:n.-16+368_-16+369delinsGT
ENST00000393585.6:c.-208+368_-208+369delinsGT	ENSP00000377210.2:n.-208+368_-208+369delinsGT
ENST00000393588.8:c.-16+1298_-16+1299delinsGT	ENSP00000377213.4:n.-16+1298_-16+1299delinsGT
ENST00000447121.2:c.-16+406_-16+407delinsGT	ENSP00000407142.2:n.-16+406_-16+407delinsGT
ENST00000517513.5:c.-16+368_-16+369delinsGT	ENSP00000428372.1:n.-16+368_-16+369delinsGT
ENST00000523916.5:c.-16+1298_-16+1299delinsGT	ENSP00000428929.1:n.-16+1298_-16+1299delinsGT
ENST00000613118.4:c.-181+368_-181+369delinsGT	ENSP00000478339.1:n.-181+368_-181+369delinsGT
NM_004346.3:c.-16+368_-16+369delinsGT	NP_004337.2:n.-16+368_-16+369delinsGT
NM_032991.2:c.-16+1298_-16+1299delinsGT	NP_116786.1:n.-16+1298_-16+1299delinsGT
XM_011532301.1:c.-16+406_-16+407delinsGT	XP_011530603.1:n.-16+406_-16+407delinsGT
NM_001354777.1:c.-16+406_-16+407delinsGT	NP_001341706.1:n.-16+406_-16+407delinsGT
NM_001354779.1:c.-90+1298_-90+1299delinsGT	NP_001341708.1:n.-90+1298_-90+1299delinsGT
NM_001354780.1:c.-90+368_-90+369delinsGT	NP_001341709.1:n.-90+368_-90+369delinsGT
NM_001354781.1:c.-16+1298_-16+1299delinsGT	NP_001341710.1:n.-16+1298_-16+1299delinsGT
NM_001354782.1:c.-16+368_-16+369delinsGT	NP_001341711.1:n.-16+368_-16+369delinsGT
NM_001354783.1:c.-181+368_-181+369delinsGT	NP_001341712.1:n.-181+368_-181+369delinsGT
NM_001354784.1:c.-90+1298_-90+1299delinsGT	NP_001341713.1:n.-90+1298_-90+1299delinsGT
NM_004346.4:c.-16+368_-16+369delinsGT MANE Select	NP_004337.2:n.-16+368_-16+369delinsGT
NM_001354777.2:c.-16+406_-16+407delinsGT	NP_001341706.1:n.-16+406_-16+407delinsGT
NM_001354779.2:c.-90+1298_-90+1299delinsGT	NP_001341708.1:n.-90+1298_-90+1299delinsGT
NM_001354780.2:c.-90+368_-90+369delinsGT	NP_001341709.1:n.-90+368_-90+369delinsGT
NM_001354781.2:c.-16+1298_-16+1299delinsGT	NP_001341710.1:n.-16+1298_-16+1299delinsGT
NM_001354782.2:c.-16+368_-16+369delinsGT	NP_001341711.1:n.-16+368_-16+369delinsGT
NM_001354783.2:c.-181+368_-181+369delinsGT	NP_001341712.1:n.-181+368_-181+369delinsGT
NM_001354784.2:c.-90+1298_-90+1299delinsGT	NP_001341713.1:n.-90+1298_-90+1299delinsGT
NM_032991.3:c.-16+1298_-16+1299delinsGT	NP_116786.1:n.-16+1298_-16+1299delinsGT