Canonical Allele Identifier: CA359105956
Gene: CASP3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.184631813C>G , CM000666.2:g.184631813C>G GRCh38
NC_000004.11:g.185552967C>G , CM000666.1:g.185552967C>G GRCh37
NC_000004.10:g.185789961C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000700100.1:c.435G>C ENSP00000514797.1:p.Gly145=
ENST00000700101.1:c.435G>C ENSP00000514798.1:p.Gly145=
ENST00000700102.1:n.503G>C
ENST00000700103.1:n.3400G>C
ENST00000700104.1:c.*184G>C ENSP00000514799.1:n.*184G>C
ENST00000308394.9:c.435G>C MANE Select ENSP00000311032.4:p.Gly145=
ENST00000308394.8:c.435G>C ENSP00000311032.4:p.Gly145=
ENST00000393585.6:c.435G>C ENSP00000377210.2:p.Gly145=
ENST00000393588.8:c.435G>C ENSP00000377213.4:p.Gly145=
ENST00000517513.5:c.435G>C ENSP00000428372.1:p.Gly145=
ENST00000523916.5:c.435G>C ENSP00000428929.1:p.Gly145=
ENST00000613118.4:c.460G>C ENSP00000478339.1:p.Gly154Arg
NM_004346.3:c.435G>C NP_004337.2:p.Gly145=
NM_032991.2:c.435G>C NP_116786.1:p.Gly145=
XM_011532301.1:c.435G>C XP_011530603.1:p.Gly145=
NM_001354777.1:c.435G>C NP_001341706.1:p.Gly145=
NM_001354779.1:c.357G>C NP_001341708.1:p.Gly119=
NM_001354780.1:c.357G>C NP_001341709.1:p.Gly119=
NM_001354781.1:c.435G>C NP_001341710.1:p.Gly145=
NM_001354782.1:c.435G>C NP_001341711.1:p.Gly145=
NM_001354783.1:c.462G>C NP_001341712.1:p.Gly154=
NM_001354784.1:c.357G>C NP_001341713.1:p.Gly119=
NM_004346.4:c.435G>C MANE Select NP_004337.2:p.Gly145=
NM_001354777.2:c.435G>C NP_001341706.1:p.Gly145=
NM_001354779.2:c.357G>C NP_001341708.1:p.Gly119=
NM_001354780.2:c.357G>C NP_001341709.1:p.Gly119=
NM_001354781.2:c.435G>C NP_001341710.1:p.Gly145=
NM_001354782.2:c.435G>C NP_001341711.1:p.Gly145=
NM_001354783.2:c.462G>C NP_001341712.1:p.Gly154=
NM_001354784.2:c.357G>C NP_001341713.1:p.Gly119=
NM_032991.3:c.435G>C NP_116786.1:p.Gly145=