Canonical Allele Identifier: CA2672813130
Gene: CASP3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.184648581G>T , CM000666.2:g.184648581G>T GRCh38
NC_000004.11:g.185569735G>T , CM000666.1:g.185569735G>T GRCh37
NC_000004.10:g.185806729G>T NCBI36
NG_051582.1:g.3969G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000700100.1:c.-132C>A ENSP00000514797.1:n.-132C>A
ENST00000700101.1:c.-16+1411C>A ENSP00000514798.1:n.-16+1411C>A
ENST00000700102.1:n.53+814C>A
ENST00000700103.1:n.53+814C>A
ENST00000700104.1:c.-16+814C>A ENSP00000514799.1:n.-16+814C>A
ENST00000308394.9:c.-132C>A MANE Select ENSP00000311032.4:n.-132C>A
ENST00000308394.8:c.-132C>A ENSP00000311032.4:n.-132C>A
ENST00000393585.6:c.-324C>A ENSP00000377210.2:n.-324C>A
ENST00000393588.8:c.-16+814C>A ENSP00000377213.4:n.-16+814C>A
ENST00000447121.2:c.-94C>A ENSP00000407142.2:n.-94C>A
ENST00000517513.5:c.-132C>A ENSP00000428372.1:n.-132C>A
ENST00000523916.5:c.-16+814C>A ENSP00000428929.1:n.-16+814C>A
ENST00000613118.4:c.-297C>A ENSP00000478339.1:n.-297C>A
NM_004346.3:c.-132C>A NP_004337.2:n.-132C>A
NM_032991.2:c.-16+814C>A NP_116786.1:n.-16+814C>A
XM_011532301.1:c.-94C>A XP_011530603.1:n.-94C>A
NM_001354777.1:c.-94C>A NP_001341706.1:n.-94C>A
NM_001354779.1:c.-90+814C>A NP_001341708.1:n.-90+814C>A
NM_001354780.1:c.-206C>A NP_001341709.1:n.-206C>A
NM_001354781.1:c.-16+814C>A NP_001341710.1:n.-16+814C>A
NM_001354782.1:c.-132C>A NP_001341711.1:n.-132C>A
NM_001354783.1:c.-297C>A NP_001341712.1:n.-297C>A
NM_001354784.1:c.-90+814C>A NP_001341713.1:n.-90+814C>A
NM_004346.4:c.-132C>A MANE Select NP_004337.2:n.-132C>A
NM_001354777.2:c.-94C>A NP_001341706.1:n.-94C>A
NM_001354779.2:c.-90+814C>A NP_001341708.1:n.-90+814C>A
NM_001354780.2:c.-206C>A NP_001341709.1:n.-206C>A
NM_001354781.2:c.-16+814C>A NP_001341710.1:n.-16+814C>A
NM_001354782.2:c.-132C>A NP_001341711.1:n.-132C>A
NM_001354783.2:c.-297C>A NP_001341712.1:n.-297C>A
NM_001354784.2:c.-90+814C>A NP_001341713.1:n.-90+814C>A
NM_032991.3:c.-16+814C>A NP_116786.1:n.-16+814C>A