Canonical Allele Identifier: CA2332698577

Gene: PEPD

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33387467C= , CM000681.2:g.33387467C=	GRCh38
NC_000019.9:g.33878373C= , CM000681.1:g.33878373C=	GRCh37
NC_000019.8:g.38570213C=	NCBI36
NG_013358.1:g.139427G=
NG_013358.2:g.139427G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.1425G=	ENSP00000468516.4:p.Glu475=
ENST00000651901.2:c.1449G=	ENSP00000498922.2:p.Glu483=
ENST00000698359.1:c.1314G=	ENSP00000513682.1:p.Glu438=
ENST00000698360.1:c.1410G=	ENSP00000513683.1:p.Glu470=
ENST00000698361.1:c.1475G=	ENSP00000513684.1:p.Arg492=
ENST00000698362.1:c.*496G=	ENSP00000513685.1:n.*496G=
ENST00000698426.1:c.1038G=	ENSP00000513713.1:p.Glu346=
ENST00000698427.1:c.1401G=	ENSP00000513714.1:p.Glu467=
ENST00000698428.1:c.1038G=	ENSP00000513715.1:p.Glu346=
ENST00000698429.1:n.1242G=
ENST00000698430.1:c.1609G=
ENST00000698431.1:c.1096G=	ENSP00000513717.1:n.1096G=
ENST00000698432.1:c.1168G=
ENST00000698433.1:n.821G=
ENST00000244137.12:c.1359G= MANE Select	ENSP00000244137.5:p.Glu453=
ENST00000588328.6:c.1414G=
ENST00000651901.1:c.1445G=
ENST00000244137.11:c.1359G=	ENSP00000244137.5:p.Glu453=
ENST00000397032.8:c.1236G=	ENSP00000380226.3:p.Glu412=
ENST00000436370.7:c.1167G=	ENSP00000391890.2:p.Glu389=
ENST00000589598.5:n.84G=
ENST00000591968.1:n.431G=
ENST00000593085.1:n.1246G=
NM_000285.3:c.1359G=	NP_000276.2:p.Glu453=
NM_001166056.1:c.1236G=	NP_001159528.1:p.Glu412=
NM_001166057.1:c.1167G=	NP_001159529.1:p.Glu389=
NM_000285.4:c.1359G= MANE Select	NP_000276.2:p.Glu453=
NM_001166056.2:c.1236G=	NP_001159528.1:p.Glu412=
NM_001166057.2:c.1167G=	NP_001159529.1:p.Glu389=