Canonical Allele Identifier: CA1519162145

Gene: CASP3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.184648830_184648835delinsACCGCT , CM000666.2:g.184648830_184648835delinsACCGCT	GRCh38
NC_000004.11:g.185569984_185569989delinsACCGCT , CM000666.1:g.185569984_185569989delinsACCGCT	GRCh37
NC_000004.10:g.185806978_185806983delinsACCGCT	NCBI36
NG_051582.1:g.4218_4223delinsACCGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700100.1:c.-386_-381delinsAGCGGT	ENSP00000514797.1:n.-386_-381delinsAGCGGT
ENST00000700101.1:c.-16+1157_-16+1162delinsAGCGGT	ENSP00000514798.1:n.-16+1157_-16+1162delinsAGCGGT
ENST00000700102.1:n.53+560_53+565delinsAGCGGT
ENST00000700103.1:n.53+560_53+565delinsAGCGGT
ENST00000700104.1:c.-16+560_-16+565delinsAGCGGT	ENSP00000514799.1:n.-16+560_-16+565delinsAGCGGT
ENST00000308394.9:c.-182-204_-182-199delinsAGCGGT MANE Select	ENSP00000311032.4:n.-182-204_-182-199delinsAGCGGT
ENST00000308394.8:c.-182-204_-182-199delinsAGCGGT	ENSP00000311032.4:n.-182-204_-182-199delinsAGCGGT
ENST00000393588.8:c.-16+560_-16+565delinsAGCGGT	ENSP00000377213.4:n.-16+560_-16+565delinsAGCGGT
ENST00000447121.2:c.-144-204_-144-199delinsAGCGGT	ENSP00000407142.2:n.-144-204_-144-199delinsAGCGGT
ENST00000517513.5:c.-182-204_-182-199delinsAGCGGT	ENSP00000428372.1:n.-182-204_-182-199delinsAGCGGT
ENST00000523916.5:c.-16+560_-16+565delinsAGCGGT	ENSP00000428929.1:n.-16+560_-16+565delinsAGCGGT
NM_004346.3:c.-182-204_-182-199delinsAGCGGT	NP_004337.2:n.-182-204_-182-199delinsAGCGGT
NM_032991.2:c.-16+560_-16+565delinsAGCGGT	NP_116786.1:n.-16+560_-16+565delinsAGCGGT
XM_011532301.1:c.-144-204_-144-199delinsAGCGGT	XP_011530603.1:n.-144-204_-144-199delinsAGCGGT
NM_001354777.1:c.-144-204_-144-199delinsAGCGGT	NP_001341706.1:n.-144-204_-144-199delinsAGCGGT
NM_001354779.1:c.-90+560_-90+565delinsAGCGGT	NP_001341708.1:n.-90+560_-90+565delinsAGCGGT
NM_001354780.1:c.-256-204_-256-199delinsAGCGGT	NP_001341709.1:n.-256-204_-256-199delinsAGCGGT
NM_001354781.1:c.-16+560_-16+565delinsAGCGGT	NP_001341710.1:n.-16+560_-16+565delinsAGCGGT
NM_001354782.1:c.-182-204_-182-199delinsAGCGGT	NP_001341711.1:n.-182-204_-182-199delinsAGCGGT
NM_001354783.1:c.-347-204_-347-199delinsAGCGGT	NP_001341712.1:n.-347-204_-347-199delinsAGCGGT
NM_001354784.1:c.-90+560_-90+565delinsAGCGGT	NP_001341713.1:n.-90+560_-90+565delinsAGCGGT
NM_004346.4:c.-182-204_-182-199delinsAGCGGT MANE Select	NP_004337.2:n.-182-204_-182-199delinsAGCGGT
NM_001354777.2:c.-144-204_-144-199delinsAGCGGT	NP_001341706.1:n.-144-204_-144-199delinsAGCGGT
NM_001354779.2:c.-90+560_-90+565delinsAGCGGT	NP_001341708.1:n.-90+560_-90+565delinsAGCGGT
NM_001354780.2:c.-256-204_-256-199delinsAGCGGT	NP_001341709.1:n.-256-204_-256-199delinsAGCGGT
NM_001354781.2:c.-16+560_-16+565delinsAGCGGT	NP_001341710.1:n.-16+560_-16+565delinsAGCGGT
NM_001354782.2:c.-182-204_-182-199delinsAGCGGT	NP_001341711.1:n.-182-204_-182-199delinsAGCGGT
NM_001354783.2:c.-347-204_-347-199delinsAGCGGT	NP_001341712.1:n.-347-204_-347-199delinsAGCGGT
NM_001354784.2:c.-90+560_-90+565delinsAGCGGT	NP_001341713.1:n.-90+560_-90+565delinsAGCGGT
NM_032991.3:c.-16+560_-16+565delinsAGCGGT	NP_116786.1:n.-16+560_-16+565delinsAGCGGT