Canonical Allele Identifier: CA1519162116

Gene: CASP3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.184648808_184648809delinsCG , CM000666.2:g.184648808_184648809delinsCG	GRCh38
NC_000004.11:g.185569962_185569963delinsCG , CM000666.1:g.185569962_185569963delinsCG	GRCh37
NC_000004.10:g.185806956_185806957delinsCG	NCBI36
NG_051582.1:g.4196_4197delinsCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000700100.1:c.-360_-359delinsCG	ENSP00000514797.1:n.-360_-359delinsCG
ENST00000700101.1:c.-16+1183_-16+1184delinsCG	ENSP00000514798.1:n.-16+1183_-16+1184delinsCG
ENST00000700102.1:n.53+586_53+587delinsCG
ENST00000700103.1:n.53+586_53+587delinsCG
ENST00000700104.1:c.-16+586_-16+587delinsCG	ENSP00000514799.1:n.-16+586_-16+587delinsCG
ENST00000308394.9:c.-182-178_-182-177delinsCG MANE Select	ENSP00000311032.4:n.-182-178_-182-177delinsCG
ENST00000308394.8:c.-182-178_-182-177delinsCG	ENSP00000311032.4:n.-182-178_-182-177delinsCG
ENST00000393588.8:c.-16+586_-16+587delinsCG	ENSP00000377213.4:n.-16+586_-16+587delinsCG
ENST00000447121.2:c.-144-178_-144-177delinsCG	ENSP00000407142.2:n.-144-178_-144-177delinsCG
ENST00000517513.5:c.-182-178_-182-177delinsCG	ENSP00000428372.1:n.-182-178_-182-177delinsCG
ENST00000523916.5:c.-16+586_-16+587delinsCG	ENSP00000428929.1:n.-16+586_-16+587delinsCG
NM_004346.3:c.-182-178_-182-177delinsCG	NP_004337.2:n.-182-178_-182-177delinsCG
NM_032991.2:c.-16+586_-16+587delinsCG	NP_116786.1:n.-16+586_-16+587delinsCG
XM_011532301.1:c.-144-178_-144-177delinsCG	XP_011530603.1:n.-144-178_-144-177delinsCG
NM_001354777.1:c.-144-178_-144-177delinsCG	NP_001341706.1:n.-144-178_-144-177delinsCG
NM_001354779.1:c.-90+586_-90+587delinsCG	NP_001341708.1:n.-90+586_-90+587delinsCG
NM_001354780.1:c.-256-178_-256-177delinsCG	NP_001341709.1:n.-256-178_-256-177delinsCG
NM_001354781.1:c.-16+586_-16+587delinsCG	NP_001341710.1:n.-16+586_-16+587delinsCG
NM_001354782.1:c.-182-178_-182-177delinsCG	NP_001341711.1:n.-182-178_-182-177delinsCG
NM_001354783.1:c.-347-178_-347-177delinsCG	NP_001341712.1:n.-347-178_-347-177delinsCG
NM_001354784.1:c.-90+586_-90+587delinsCG	NP_001341713.1:n.-90+586_-90+587delinsCG
NM_004346.4:c.-182-178_-182-177delinsCG MANE Select	NP_004337.2:n.-182-178_-182-177delinsCG
NM_001354777.2:c.-144-178_-144-177delinsCG	NP_001341706.1:n.-144-178_-144-177delinsCG
NM_001354779.2:c.-90+586_-90+587delinsCG	NP_001341708.1:n.-90+586_-90+587delinsCG
NM_001354780.2:c.-256-178_-256-177delinsCG	NP_001341709.1:n.-256-178_-256-177delinsCG
NM_001354781.2:c.-16+586_-16+587delinsCG	NP_001341710.1:n.-16+586_-16+587delinsCG
NM_001354782.2:c.-182-178_-182-177delinsCG	NP_001341711.1:n.-182-178_-182-177delinsCG
NM_001354783.2:c.-347-178_-347-177delinsCG	NP_001341712.1:n.-347-178_-347-177delinsCG
NM_001354784.2:c.-90+586_-90+587delinsCG	NP_001341713.1:n.-90+586_-90+587delinsCG
NM_032991.3:c.-16+586_-16+587delinsCG	NP_116786.1:n.-16+586_-16+587delinsCG