Canonical Allele Identifier: CA2332698571

Gene: PEPD

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33387460C= , CM000681.2:g.33387460C=	GRCh38
NC_000019.9:g.33878366C= , CM000681.1:g.33878366C=	GRCh37
NC_000019.8:g.38570206C=	NCBI36
NG_013358.1:g.139434G=
NG_013358.2:g.139434G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.1432G=	ENSP00000468516.4:p.Val478=
ENST00000651901.2:c.1456G=	ENSP00000498922.2:p.Val486=
ENST00000698359.1:c.1321G=	ENSP00000513682.1:p.Val441=
ENST00000698360.1:c.1417G=	ENSP00000513683.1:p.Val473=
ENST00000698361.1:c.1482G=	ENSP00000513684.1:p.Ser494=
ENST00000698362.1:c.*503G=	ENSP00000513685.1:n.*503G=
ENST00000698426.1:c.1045G=	ENSP00000513713.1:p.Val349=
ENST00000698427.1:c.1408G=	ENSP00000513714.1:p.Val470=
ENST00000698428.1:c.1045G=	ENSP00000513715.1:p.Val349=
ENST00000698429.1:n.1249G=
ENST00000698430.1:c.1616G=
ENST00000698431.1:c.1103G=	ENSP00000513717.1:n.1103G=
ENST00000698432.1:c.1175G=
ENST00000698433.1:n.828G=
ENST00000244137.12:c.1366G= MANE Select	ENSP00000244137.5:p.Val456=
ENST00000588328.6:c.1421G=
ENST00000651901.1:c.1452G=
ENST00000244137.11:c.1366G=	ENSP00000244137.5:p.Val456=
ENST00000397032.8:c.1243G=	ENSP00000380226.3:p.Val415=
ENST00000436370.7:c.1174G=	ENSP00000391890.2:p.Val392=
ENST00000589598.5:n.91G=
ENST00000591968.1:n.438G=
ENST00000593085.1:n.1253G=
NM_000285.3:c.1366G=	NP_000276.2:p.Val456=
NM_001166056.1:c.1243G=	NP_001159528.1:p.Val415=
NM_001166057.1:c.1174G=	NP_001159529.1:p.Val392=
NM_000285.4:c.1366G= MANE Select	NP_000276.2:p.Val456=
NM_001166056.2:c.1243G=	NP_001159528.1:p.Val415=
NM_001166057.2:c.1174G=	NP_001159529.1:p.Val392=