Canonical Allele Identifier: CA2576746826

Gene: PEPD

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33463900A>C , CM000681.2:g.33463900A>C	GRCh38
NC_000019.9:g.33954806A>C , CM000681.1:g.33954806A>C	GRCh37
NC_000019.8:g.38646646A>C	NCBI36
NG_013358.1:g.62994T>G
NG_013358.2:g.62994T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.624+87T>G	ENSP00000468516.4:n.624+87T>G
ENST00000651646.2:c.624+87T>G	ENSP00000498950.2:n.624+87T>G
ENST00000651901.2:c.624+87T>G	ENSP00000498922.2:n.624+87T>G
ENST00000698359.1:c.579+87T>G	ENSP00000513682.1:n.579+87T>G
ENST00000698360.1:c.624+87T>G	ENSP00000513683.1:n.624+87T>G
ENST00000698361.1:c.624+87T>G	ENSP00000513684.1:n.624+87T>G
ENST00000698362.1:c.624+87T>G	ENSP00000513685.1:n.624+87T>G
ENST00000698363.1:n.687+87T>G
ENST00000698364.1:n.687+87T>G
ENST00000698365.1:n.687+87T>G
ENST00000698426.1:c.303+87T>G	ENSP00000513713.1:n.303+87T>G
ENST00000698427.1:c.666+87T>G	ENSP00000513714.1:n.666+87T>G
ENST00000698428.1:c.303+87T>G	ENSP00000513715.1:n.303+87T>G
ENST00000698430.1:c.874+87T>G
ENST00000698431.1:c.361+87T>G	ENSP00000513717.1:n.361+87T>G
ENST00000698432.1:c.433+87T>G
ENST00000698435.1:c.312+87T>G	ENSP00000513719.1:n.312+87T>G
ENST00000698436.1:c.*236+87T>G	ENSP00000513720.1:n.*236+87T>G
ENST00000698437.1:n.607+87T>G
ENST00000698438.1:n.606+87T>G
ENST00000698439.1:c.481+87T>G	ENSP00000513721.1:n.481+87T>G
ENST00000244137.12:c.624+87T>G MANE Select	ENSP00000244137.5:n.624+87T>G
ENST00000588328.6:c.613+87T>G
ENST00000590731.6:n.299+87T>G
ENST00000651646.1:c.622+87T>G
ENST00000651901.1:c.620+87T>G
ENST00000244137.11:c.624+87T>G	ENSP00000244137.5:n.624+87T>G
ENST00000397032.8:c.548+14146T>G	ENSP00000380226.3:n.548+14146T>G
ENST00000436370.7:c.432+87T>G	ENSP00000391890.2:n.432+87T>G
ENST00000588328.5:c.115+87T>G
ENST00000588719.5:n.259+87T>G
ENST00000590408.1:c.342+87T>G
ENST00000590731.5:n.299+87T>G
ENST00000590755.6:c.451+87T>G	ENSP00000476667.1:n.451+87T>G
ENST00000593163.5:n.789+87T>G
ENST00000609145.5:c.57+87T>G	ENSP00000476514.1:n.57+87T>G
NM_000285.3:c.624+87T>G	NP_000276.2:n.624+87T>G
NM_001166056.1:c.548+14146T>G	NP_001159528.1:n.548+14146T>G
NM_001166057.1:c.432+87T>G	NP_001159529.1:n.432+87T>G
NM_000285.4:c.624+87T>G MANE Select	NP_000276.2:n.624+87T>G
NM_001166056.2:c.548+14146T>G	NP_001159528.1:n.548+14146T>G
NM_001166057.2:c.432+87T>G	NP_001159529.1:n.432+87T>G