Canonical Allele Identifier: CA2672813026
Gene: CASP3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.184648494C>T , CM000666.2:g.184648494C>T GRCh38
NC_000004.11:g.185569648C>T , CM000666.1:g.185569648C>T GRCh37
NC_000004.10:g.185806642C>T NCBI36
NG_051582.1:g.3882C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000700100.1:c.-45G>A ENSP00000514797.1:n.-45G>A
ENST00000700101.1:c.-16+1498G>A ENSP00000514798.1:n.-16+1498G>A
ENST00000700102.1:n.53+901G>A
ENST00000700103.1:n.53+901G>A
ENST00000700104.1:c.-16+901G>A ENSP00000514799.1:n.-16+901G>A
ENST00000308394.9:c.-45G>A MANE Select ENSP00000311032.4:n.-45G>A
ENST00000308394.8:c.-45G>A ENSP00000311032.4:n.-45G>A
ENST00000393585.6:c.-237G>A ENSP00000377210.2:n.-237G>A
ENST00000393588.8:c.-16+901G>A ENSP00000377213.4:n.-16+901G>A
ENST00000447121.2:c.-16+9G>A ENSP00000407142.2:n.-16+9G>A
ENST00000517513.5:c.-45G>A ENSP00000428372.1:n.-45G>A
ENST00000523916.5:c.-16+901G>A ENSP00000428929.1:n.-16+901G>A
ENST00000613118.4:c.-210G>A ENSP00000478339.1:n.-210G>A
NM_004346.3:c.-45G>A NP_004337.2:n.-45G>A
NM_032991.2:c.-16+901G>A NP_116786.1:n.-16+901G>A
XM_011532301.1:c.-16+9G>A XP_011530603.1:n.-16+9G>A
NM_001354777.1:c.-16+9G>A NP_001341706.1:n.-16+9G>A
NM_001354779.1:c.-90+901G>A NP_001341708.1:n.-90+901G>A
NM_001354780.1:c.-119G>A NP_001341709.1:n.-119G>A
NM_001354781.1:c.-16+901G>A NP_001341710.1:n.-16+901G>A
NM_001354782.1:c.-45G>A NP_001341711.1:n.-45G>A
NM_001354783.1:c.-210G>A NP_001341712.1:n.-210G>A
NM_001354784.1:c.-90+901G>A NP_001341713.1:n.-90+901G>A
NM_004346.4:c.-45G>A MANE Select NP_004337.2:n.-45G>A
NM_001354777.2:c.-16+9G>A NP_001341706.1:n.-16+9G>A
NM_001354779.2:c.-90+901G>A NP_001341708.1:n.-90+901G>A
NM_001354780.2:c.-119G>A NP_001341709.1:n.-119G>A
NM_001354781.2:c.-16+901G>A NP_001341710.1:n.-16+901G>A
NM_001354782.2:c.-45G>A NP_001341711.1:n.-45G>A
NM_001354783.2:c.-210G>A NP_001341712.1:n.-210G>A
NM_001354784.2:c.-90+901G>A NP_001341713.1:n.-90+901G>A
NM_032991.3:c.-16+901G>A NP_116786.1:n.-16+901G>A