Canonical Allele Identifier: CA11711356
Gene: CASP3 HGNC NCBI

Linked Data

dbSNP Id: rs113420705

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.184649399T>C , CM000666.2:g.184649399T>C GRCh38
NC_000004.11:g.185570553T>C , CM000666.1:g.185570553T>C GRCh37
NC_000004.10:g.185807547T>C NCBI36
NG_051582.1:g.4787T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000308394.9:c.-187A>G MANE Select ENSP00000311032.4:p.=
ENST00000308394.8:c.-187A>G ENSP00000311032.4:p.=
ENST00000393588.8:c.-20A>G ENSP00000377213.4:p.=
ENST00000447121.2:c.-149A>G ENSP00000407142.2:p.=
ENST00000517513.5:c.-187A>G ENSP00000428372.1:p.=
ENST00000523916.5:c.-20A>G ENSP00000428929.1:p.=
NM_004346.3:c.-187A>G NP_004337.2:p.=
NM_032991.2:c.-20A>G NP_116786.1:p.=
XM_011532301.1:c.-149A>G XP_011530603.1:p.=
NM_001354777.1:c.-149A>G NP_001341706.1:p.=
NM_001354779.1:c.-94A>G NP_001341708.1:p.=
NM_001354780.1:c.-261A>G NP_001341709.1:p.=
NM_001354781.1:c.-20A>G NP_001341710.1:p.=
NM_001354782.1:c.-187A>G NP_001341711.1:p.=
NM_001354783.1:c.-352A>G NP_001341712.1:p.=
NM_001354784.1:c.-94A>G NP_001341713.1:p.=
NM_004346.4:c.-187A>G MANE Select NP_004337.2:p.=
NM_001354777.2:c.-149A>G NP_001341706.1:p.=
NM_001354779.2:c.-94A>G NP_001341708.1:p.=
NM_001354780.2:c.-261A>G NP_001341709.1:p.=
NM_001354781.2:c.-20A>G NP_001341710.1:p.=
NM_001354782.2:c.-187A>G NP_001341711.1:p.=
NM_001354783.2:c.-352A>G NP_001341712.1:p.=
NM_001354784.2:c.-94A>G NP_001341713.1:p.=
NM_032991.3:c.-20A>G NP_116786.1:p.=