Canonical Allele Identifier: CA405230840
Gene: PEPD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33464062G>T , CM000681.2:g.33464062G>T GRCh38
NC_000019.9:g.33954968G>T , CM000681.1:g.33954968G>T GRCh37
NC_000019.8:g.38646808G>T NCBI36
NG_013358.1:g.62832C>A
NG_013358.2:g.62832C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000588328.7:c.549C>A ENSP00000468516.4:p.Cys183Ter
ENST00000651646.2:c.549C>A ENSP00000498950.2:p.Cys183Ter
ENST00000651901.2:c.549C>A ENSP00000498922.2:p.Cys183Ter
ENST00000698359.1:c.504C>A ENSP00000513682.1:p.Asn168Lys
ENST00000698360.1:c.549C>A ENSP00000513683.1:p.Cys183Ter
ENST00000698361.1:c.549C>A ENSP00000513684.1:p.Cys183Ter
ENST00000698362.1:c.549C>A ENSP00000513685.1:p.Cys183Ter
ENST00000698363.1:n.612C>A
ENST00000698364.1:n.612C>A
ENST00000698365.1:n.612C>A
ENST00000698426.1:c.228C>A ENSP00000513713.1:p.Cys76Ter
ENST00000698427.1:c.591C>A ENSP00000513714.1:p.Cys197Ter
ENST00000698428.1:c.228C>A ENSP00000513715.1:p.Cys76Ter
ENST00000698430.1:c.799C>A
ENST00000698431.1:c.286C>A ENSP00000513717.1:n.286C>A
ENST00000698432.1:c.358C>A
ENST00000698435.1:c.237C>A ENSP00000513719.1:p.Cys79Ter
ENST00000698436.1:c.*161C>A ENSP00000513720.1:n.*161C>A
ENST00000698437.1:n.532C>A
ENST00000698438.1:n.531C>A
ENST00000698439.1:c.406C>A ENSP00000513721.1:n.406C>A
ENST00000244137.12:c.549C>A MANE Select ENSP00000244137.5:p.Cys183Ter
ENST00000588328.6:c.538C>A
ENST00000590731.6:n.224C>A
ENST00000651646.1:c.547C>A
ENST00000651901.1:c.545C>A
ENST00000244137.11:c.549C>A ENSP00000244137.5:p.Cys183Ter
ENST00000397032.8:c.548+13984C>A ENSP00000380226.3:n.548+13984C>A
ENST00000436370.7:c.357C>A ENSP00000391890.2:p.Cys119Ter
ENST00000588328.5:c.40C>A
ENST00000588719.5:n.184C>A
ENST00000590408.1:c.267C>A
ENST00000590731.5:n.224C>A
ENST00000590755.6:c.376C>A ENSP00000476667.1:n.376C>A
ENST00000593163.5:n.714C>A
ENST00000609145.5:c.-19C>A ENSP00000476514.1:n.-19C>A
NM_000285.3:c.549C>A NP_000276.2:p.Cys183Ter
NM_001166056.1:c.548+13984C>A NP_001159528.1:n.548+13984C>A
NM_001166057.1:c.357C>A NP_001159529.1:p.Cys119Ter
NM_000285.4:c.549C>A MANE Select NP_000276.2:p.Cys183Ter
NM_001166056.2:c.548+13984C>A NP_001159528.1:n.548+13984C>A
NM_001166057.2:c.357C>A NP_001159529.1:p.Cys119Ter