Canonical Allele Identifier: CA2332698573

Gene: PEPD

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33387463C= , CM000681.2:g.33387463C=	GRCh38
NC_000019.9:g.33878369C= , CM000681.1:g.33878369C=	GRCh37
NC_000019.8:g.38570209C=	NCBI36
NG_013358.1:g.139431G=
NG_013358.2:g.139431G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.1429G=	ENSP00000468516.4:p.Val477=
ENST00000651901.2:c.1453G=	ENSP00000498922.2:p.Val485=
ENST00000698359.1:c.1318G=	ENSP00000513682.1:p.Val440=
ENST00000698360.1:c.1414G=	ENSP00000513683.1:p.Val472=
ENST00000698361.1:c.1479G=	ENSP00000513684.1:p.Thr493=
ENST00000698362.1:c.*500G=	ENSP00000513685.1:n.*500G=
ENST00000698426.1:c.1042G=	ENSP00000513713.1:p.Val348=
ENST00000698427.1:c.1405G=	ENSP00000513714.1:p.Val469=
ENST00000698428.1:c.1042G=	ENSP00000513715.1:p.Val348=
ENST00000698429.1:n.1246G=
ENST00000698430.1:c.1613G=
ENST00000698431.1:c.1100G=	ENSP00000513717.1:n.1100G=
ENST00000698432.1:c.1172G=
ENST00000698433.1:n.825G=
ENST00000244137.12:c.1363G= MANE Select	ENSP00000244137.5:p.Val455=
ENST00000588328.6:c.1418G=
ENST00000651901.1:c.1449G=
ENST00000244137.11:c.1363G=	ENSP00000244137.5:p.Val455=
ENST00000397032.8:c.1240G=	ENSP00000380226.3:p.Val414=
ENST00000436370.7:c.1171G=	ENSP00000391890.2:p.Val391=
ENST00000589598.5:n.88G=
ENST00000591968.1:n.435G=
ENST00000593085.1:n.1250G=
NM_000285.3:c.1363G=	NP_000276.2:p.Val455=
NM_001166056.1:c.1240G=	NP_001159528.1:p.Val414=
NM_001166057.1:c.1171G=	NP_001159529.1:p.Val391=
NM_000285.4:c.1363G= MANE Select	NP_000276.2:p.Val455=
NM_001166056.2:c.1240G=	NP_001159528.1:p.Val414=
NM_001166057.2:c.1171G=	NP_001159529.1:p.Val391=