Canonical Allele Identifier: CA2332735579
Gene: PEPD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33463856G= , CM000681.2:g.33463856G= GRCh38
NC_000019.9:g.33954762G= , CM000681.1:g.33954762G= GRCh37
NC_000019.8:g.38646602G= NCBI36
NG_013358.1:g.63038C=
NG_013358.2:g.63038C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000588328.7:c.624+131C= ENSP00000468516.4:n.624+131C=
ENST00000651646.2:c.624+131C= ENSP00000498950.2:n.624+131C=
ENST00000651901.2:c.624+131C= ENSP00000498922.2:n.624+131C=
ENST00000698359.1:c.579+131C= ENSP00000513682.1:n.579+131C=
ENST00000698360.1:c.624+131C= ENSP00000513683.1:n.624+131C=
ENST00000698361.1:c.624+131C= ENSP00000513684.1:n.624+131C=
ENST00000698362.1:c.624+131C= ENSP00000513685.1:n.624+131C=
ENST00000698363.1:n.687+131C=
ENST00000698364.1:n.687+131C=
ENST00000698365.1:n.687+131C=
ENST00000698426.1:c.303+131C= ENSP00000513713.1:n.303+131C=
ENST00000698427.1:c.666+131C= ENSP00000513714.1:n.666+131C=
ENST00000698428.1:c.303+131C= ENSP00000513715.1:n.303+131C=
ENST00000698430.1:c.874+131C=
ENST00000698431.1:c.361+131C= ENSP00000513717.1:n.361+131C=
ENST00000698432.1:c.433+131C=
ENST00000698435.1:c.312+131C= ENSP00000513719.1:n.312+131C=
ENST00000698436.1:c.*236+131C= ENSP00000513720.1:n.*236+131C=
ENST00000698437.1:n.607+131C=
ENST00000698438.1:n.606+131C=
ENST00000698439.1:c.481+131C= ENSP00000513721.1:n.481+131C=
ENST00000244137.12:c.624+131C= MANE Select ENSP00000244137.5:n.624+131C=
ENST00000588328.6:c.613+131C=
ENST00000590731.6:n.299+131C=
ENST00000651646.1:c.622+131C=
ENST00000651901.1:c.620+131C=
ENST00000244137.11:c.624+131C= ENSP00000244137.5:n.624+131C=
ENST00000397032.8:c.548+14190C= ENSP00000380226.3:n.548+14190C=
ENST00000436370.7:c.432+131C= ENSP00000391890.2:n.432+131C=
ENST00000588328.5:c.115+131C=
ENST00000588719.5:n.259+131C=
ENST00000590408.1:c.342+131C=
ENST00000590731.5:n.299+131C=
ENST00000590755.6:c.451+131C= ENSP00000476667.1:n.451+131C=
ENST00000593163.5:n.789+131C=
ENST00000609145.5:c.57+131C= ENSP00000476514.1:n.57+131C=
NM_000285.3:c.624+131C= NP_000276.2:n.624+131C=
NM_001166056.1:c.548+14190C= NP_001159528.1:n.548+14190C=
NM_001166057.1:c.432+131C= NP_001159529.1:n.432+131C=
NM_000285.4:c.624+131C= MANE Select NP_000276.2:n.624+131C=
NM_001166056.2:c.548+14190C= NP_001159528.1:n.548+14190C=
NM_001166057.2:c.432+131C= NP_001159529.1:n.432+131C=