Canonical Allele Identifier: CA2332698585

Gene: PEPD

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33387480A= , CM000681.2:g.33387480A=	GRCh38
NC_000019.9:g.33878386A= , CM000681.1:g.33878386A=	GRCh37
NC_000019.8:g.38570226A=	NCBI36
NG_013358.1:g.139414T=
NG_013358.2:g.139414T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.1412T=	ENSP00000468516.4:p.Val471=
ENST00000651901.2:c.1436T=	ENSP00000498922.2:p.Val479=
ENST00000698359.1:c.1301T=	ENSP00000513682.1:p.Val434=
ENST00000698360.1:c.1397T=	ENSP00000513683.1:p.Val466=
ENST00000698361.1:c.1462T=	ENSP00000513684.1:p.Ser488=
ENST00000698362.1:c.*483T=	ENSP00000513685.1:n.*483T=
ENST00000698426.1:c.1025T=	ENSP00000513713.1:p.Val342=
ENST00000698427.1:c.1388T=	ENSP00000513714.1:p.Val463=
ENST00000698428.1:c.1025T=	ENSP00000513715.1:p.Val342=
ENST00000698429.1:n.1229T=
ENST00000698430.1:c.1596T=
ENST00000698431.1:c.1083T=	ENSP00000513717.1:n.1083T=
ENST00000698432.1:c.1155T=
ENST00000698433.1:n.808T=
ENST00000244137.12:c.1346T= MANE Select	ENSP00000244137.5:p.Val449=
ENST00000588328.6:c.1401T=
ENST00000651901.1:c.1432T=
ENST00000244137.11:c.1346T=	ENSP00000244137.5:p.Val449=
ENST00000397032.8:c.1223T=	ENSP00000380226.3:p.Val408=
ENST00000436370.7:c.1154T=	ENSP00000391890.2:p.Val385=
ENST00000589598.5:n.71T=
ENST00000591968.1:n.418T=
ENST00000593085.1:n.1233T=
NM_000285.3:c.1346T=	NP_000276.2:p.Val449=
NM_001166056.1:c.1223T=	NP_001159528.1:p.Val408=
NM_001166057.1:c.1154T=	NP_001159529.1:p.Val385=
NM_000285.4:c.1346T= MANE Select	NP_000276.2:p.Val449=
NM_001166056.2:c.1223T=	NP_001159528.1:p.Val408=
NM_001166057.2:c.1154T=	NP_001159529.1:p.Val385=