Canonical Allele Identifier: CA2510216089
Gene: CASP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.184648521G>C , CM000666.2:g.184648521G>C GRCh38
NC_000004.11:g.185569675G>C , CM000666.1:g.185569675G>C GRCh37
NC_000004.10:g.185806669G>C NCBI36
NG_051582.1:g.3909G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000700100.1:c.-72C>G ENSP00000514797.1:n.-72C>G
ENST00000700101.1:c.-16+1471C>G ENSP00000514798.1:n.-16+1471C>G
ENST00000700102.1:n.53+874C>G
ENST00000700103.1:n.53+874C>G
ENST00000700104.1:c.-16+874C>G ENSP00000514799.1:n.-16+874C>G
ENST00000308394.9:c.-72C>G MANE Select ENSP00000311032.4:n.-72C>G
ENST00000308394.8:c.-72C>G ENSP00000311032.4:n.-72C>G
ENST00000393585.6:c.-264C>G ENSP00000377210.2:n.-264C>G
ENST00000393588.8:c.-16+874C>G ENSP00000377213.4:n.-16+874C>G
ENST00000447121.2:c.-34C>G ENSP00000407142.2:n.-34C>G
ENST00000517513.5:c.-72C>G ENSP00000428372.1:n.-72C>G
ENST00000523916.5:c.-16+874C>G ENSP00000428929.1:n.-16+874C>G
ENST00000613118.4:c.-237C>G ENSP00000478339.1:n.-237C>G
NM_004346.3:c.-72C>G NP_004337.2:n.-72C>G
NM_032991.2:c.-16+874C>G NP_116786.1:n.-16+874C>G
XM_011532301.1:c.-34C>G XP_011530603.1:n.-34C>G
NM_001354777.1:c.-34C>G NP_001341706.1:n.-34C>G
NM_001354779.1:c.-90+874C>G NP_001341708.1:n.-90+874C>G
NM_001354780.1:c.-146C>G NP_001341709.1:n.-146C>G
NM_001354781.1:c.-16+874C>G NP_001341710.1:n.-16+874C>G
NM_001354782.1:c.-72C>G NP_001341711.1:n.-72C>G
NM_001354783.1:c.-237C>G NP_001341712.1:n.-237C>G
NM_001354784.1:c.-90+874C>G NP_001341713.1:n.-90+874C>G
NM_004346.4:c.-72C>G MANE Select NP_004337.2:n.-72C>G
NM_001354777.2:c.-34C>G NP_001341706.1:n.-34C>G
NM_001354779.2:c.-90+874C>G NP_001341708.1:n.-90+874C>G
NM_001354780.2:c.-146C>G NP_001341709.1:n.-146C>G
NM_001354781.2:c.-16+874C>G NP_001341710.1:n.-16+874C>G
NM_001354782.2:c.-72C>G NP_001341711.1:n.-72C>G
NM_001354783.2:c.-237C>G NP_001341712.1:n.-237C>G
NM_001354784.2:c.-90+874C>G NP_001341713.1:n.-90+874C>G
NM_032991.3:c.-16+874C>G NP_116786.1:n.-16+874C>G