Canonical Allele Identifier: CA2672813016
Gene: CASP3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.184648490del , CM000666.2:g.184648490del GRCh38
NC_000004.11:g.185569644del , CM000666.1:g.185569644del GRCh37
NC_000004.10:g.185806638del NCBI36
NG_051582.1:g.3878del

Transcript Alleles

HGVS Amino-acid change
ENST00000700100.1:c.-41del ENSP00000514797.1:n.-41del
ENST00000700101.1:c.-16+1502del ENSP00000514798.1:n.-16+1502del
ENST00000700102.1:n.53+905del
ENST00000700103.1:n.53+905del
ENST00000700104.1:c.-16+905del ENSP00000514799.1:n.-16+905del
ENST00000308394.9:c.-41del MANE Select ENSP00000311032.4:n.-41del
ENST00000308394.8:c.-41del ENSP00000311032.4:n.-41del
ENST00000393585.6:c.-233del ENSP00000377210.2:n.-233del
ENST00000393588.8:c.-16+905del ENSP00000377213.4:n.-16+905del
ENST00000447121.2:c.-16+13del ENSP00000407142.2:n.-16+13del
ENST00000517513.5:c.-41del ENSP00000428372.1:n.-41del
ENST00000523916.5:c.-16+905del ENSP00000428929.1:n.-16+905del
ENST00000613118.4:c.-206del ENSP00000478339.1:n.-206del
NM_004346.3:c.-41del NP_004337.2:n.-41del
NM_032991.2:c.-16+905del NP_116786.1:n.-16+905del
XM_011532301.1:c.-16+13del XP_011530603.1:n.-16+13del
NM_001354777.1:c.-16+13del NP_001341706.1:n.-16+13del
NM_001354779.1:c.-90+905del NP_001341708.1:n.-90+905del
NM_001354780.1:c.-115del NP_001341709.1:n.-115del
NM_001354781.1:c.-16+905del NP_001341710.1:n.-16+905del
NM_001354782.1:c.-41del NP_001341711.1:n.-41del
NM_001354783.1:c.-206del NP_001341712.1:n.-206del
NM_001354784.1:c.-90+905del NP_001341713.1:n.-90+905del
NM_004346.4:c.-41del MANE Select NP_004337.2:n.-41del
NM_001354777.2:c.-16+13del NP_001341706.1:n.-16+13del
NM_001354779.2:c.-90+905del NP_001341708.1:n.-90+905del
NM_001354780.2:c.-115del NP_001341709.1:n.-115del
NM_001354781.2:c.-16+905del NP_001341710.1:n.-16+905del
NM_001354782.2:c.-41del NP_001341711.1:n.-41del
NM_001354783.2:c.-206del NP_001341712.1:n.-206del
NM_001354784.2:c.-90+905del NP_001341713.1:n.-90+905del
NM_032991.3:c.-16+905del NP_116786.1:n.-16+905del