Canonical Allele Identifier: CA11842865
Gene: CASP3 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1049253

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.184627797A>G , CM000666.2:g.184627797A>G GRCh38
NC_000004.11:g.185548951A>G , CM000666.1:g.185548951A>G GRCh37
NC_000004.10:g.185785945A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_004346.3:c.*1475T>C VV NP_004337.2:p.=
NM_032991.2:c.*1475T>C VV NP_116786.1:p.=
XM_011532301.1:c.*1475T>C XP_011530603.1:p.=
NM_001354777.1:c.*1475T>C VV NP_001341706.1:p.=
NM_001354779.1:c.*1475T>C VV NP_001341708.1:p.=
NM_001354780.1:c.*1475T>C VV NP_001341709.1:p.=
NM_001354781.1:c.*1639T>C VV NP_001341710.1:p.=
NM_001354782.1:c.*1639T>C VV NP_001341711.1:p.=
NM_001354783.1:c.*1639T>C VV NP_001341712.1:p.=
NM_001354784.1:c.*1639T>C VV NP_001341713.1:p.=
NM_004346.4:c.*1475T>C VV MANE Preferred NP_004337.2:p.=
ENST00000308394.8:c.*1475T>C ENSP00000311032.4:p.=
ENST00000393585.6:c.*1639T>C ENSP00000377210.2:p.=
ENST00000523916.5:c.*1475T>C ENSP00000428929.1:p.=
ENST00000613118.4:c.*1742T>C ENSP00000478339.1:p.=