Canonical Allele Identifier: CA405234689
Gene: PEPD HGNC NCBI

Linked Data

dbSNP Id: rs1252010868

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33521748T>C , CM000681.2:g.33521748T>C GRCh38
NC_000019.9:g.34012654T>C , CM000681.1:g.34012654T>C GRCh37
NC_000019.8:g.38704494T>C NCBI36
NG_013358.1:g.5146A>G
NG_013358.2:g.5146A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000588328.7:c.13A>G ENSP00000468516.4:p.Thr5Ala
ENST00000651646.2:c.13A>G ENSP00000498950.2:p.Thr5Ala
ENST00000651901.2:c.13A>G ENSP00000498922.2:p.Thr5Ala
ENST00000698359.1:c.13A>G ENSP00000513682.1:p.Thr5Ala
ENST00000698360.1:c.13A>G ENSP00000513683.1:p.Thr5Ala
ENST00000698361.1:c.13A>G ENSP00000513684.1:p.Thr5Ala
ENST00000698362.1:c.13A>G ENSP00000513685.1:p.Thr5Ala
ENST00000698363.1:n.76A>G
ENST00000698364.1:n.76A>G
ENST00000698365.1:n.76A>G
ENST00000698426.1:c.-503A>G ENSP00000513713.1:n.-503A>G
ENST00000698427.1:c.-53A>G ENSP00000513714.1:n.-53A>G
ENST00000698428.1:c.-381A>G ENSP00000513715.1:n.-381A>G
ENST00000698435.1:c.13A>G ENSP00000513719.1:p.Thr5Ala
ENST00000698436.1:c.13A>G ENSP00000513720.1:p.Thr5Ala
ENST00000244137.12:c.13A>G MANE Select ENSP00000244137.5:p.Thr5Ala
ENST00000588328.6:c.2A>G
ENST00000651646.1:c.11A>G
ENST00000651901.1:c.9A>G
ENST00000244137.11:c.13A>G ENSP00000244137.5:p.Thr5Ala
ENST00000397032.8:c.13A>G ENSP00000380226.3:p.Thr5Ala
ENST00000436370.7:c.13A>G ENSP00000391890.2:p.Thr5Ala
NM_000285.3:c.13A>G NP_000276.2:p.Thr5Ala
NM_001166056.1:c.13A>G NP_001159528.1:p.Thr5Ala
NM_001166057.1:c.13A>G NP_001159529.1:p.Thr5Ala
NM_000285.4:c.13A>G MANE Select NP_000276.2:p.Thr5Ala
NM_001166056.2:c.13A>G NP_001159528.1:p.Thr5Ala
NM_001166057.2:c.13A>G NP_001159529.1:p.Thr5Ala