Canonical Allele Identifier: CA15305456
Gene: CASP3 HGNC NCBI

Linked Data

dbSNP Id: rs4647693

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.184629610T>C , CM000666.2:g.184629610T>C GRCh38
NC_000004.11:g.185550764T>C , CM000666.1:g.185550764T>C GRCh37
NC_000004.10:g.185787758T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000308394.9:c.605-109A>G MANE Select ENSP00000311032.4:p.=
ENST00000308394.8:c.605-109A>G ENSP00000311032.4:p.=
ENST00000393585.6:c.484-109A>G ENSP00000377210.2:p.=
ENST00000393588.8:c.484-109A>G ENSP00000377213.4:p.=
ENST00000517513.5:c.484-109A>G ENSP00000428372.1:p.=
ENST00000523916.5:c.605-109A>G ENSP00000428929.1:p.=
ENST00000613118.4:c.*38-109A>G ENSP00000478339.1:p.=
NM_004346.3:c.605-109A>G NP_004337.2:p.=
NM_032991.2:c.605-109A>G NP_116786.1:p.=
XM_011532301.1:c.605-109A>G XP_011530603.1:p.=
NM_001354777.1:c.605-109A>G NP_001341706.1:p.=
NM_001354779.1:c.527-109A>G NP_001341708.1:p.=
NM_001354780.1:c.527-109A>G NP_001341709.1:p.=
NM_001354781.1:c.484-109A>G NP_001341710.1:p.=
NM_001354782.1:c.484-109A>G NP_001341711.1:p.=
NM_001354783.1:c.511-109A>G NP_001341712.1:p.=
NM_001354784.1:c.406-109A>G NP_001341713.1:p.=
NM_004346.4:c.605-109A>G MANE Select NP_004337.2:p.=
NM_001354777.2:c.605-109A>G NP_001341706.1:p.=
NM_001354779.2:c.527-109A>G NP_001341708.1:p.=
NM_001354780.2:c.527-109A>G NP_001341709.1:p.=
NM_001354781.2:c.484-109A>G NP_001341710.1:p.=
NM_001354782.2:c.484-109A>G NP_001341711.1:p.=
NM_001354783.2:c.511-109A>G NP_001341712.1:p.=
NM_001354784.2:c.406-109A>G NP_001341713.1:p.=
NM_032991.3:c.605-109A>G NP_116786.1:p.=