Canonical Allele Identifier: CA2332698575

Gene: PEPD

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33387464G= , CM000681.2:g.33387464G=	GRCh38
NC_000019.9:g.33878370G= , CM000681.1:g.33878370G=	GRCh37
NC_000019.8:g.38570210G=	NCBI36
NG_013358.1:g.139430C=
NG_013358.2:g.139430C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.1428C=	ENSP00000468516.4:p.Asp476=
ENST00000651901.2:c.1452C=	ENSP00000498922.2:p.Asp484=
ENST00000698359.1:c.1317C=	ENSP00000513682.1:p.Asp439=
ENST00000698360.1:c.1413C=	ENSP00000513683.1:p.Asp471=
ENST00000698361.1:c.1478C=	ENSP00000513684.1:p.Thr493=
ENST00000698362.1:c.*499C=	ENSP00000513685.1:n.*499C=
ENST00000698426.1:c.1041C=	ENSP00000513713.1:p.Asp347=
ENST00000698427.1:c.1404C=	ENSP00000513714.1:p.Asp468=
ENST00000698428.1:c.1041C=	ENSP00000513715.1:p.Asp347=
ENST00000698429.1:n.1245C=
ENST00000698430.1:c.1612C=
ENST00000698431.1:c.1099C=	ENSP00000513717.1:n.1099C=
ENST00000698432.1:c.1171C=
ENST00000698433.1:n.824C=
ENST00000244137.12:c.1362C= MANE Select	ENSP00000244137.5:p.Asp454=
ENST00000588328.6:c.1417C=
ENST00000651901.1:c.1448C=
ENST00000244137.11:c.1362C=	ENSP00000244137.5:p.Asp454=
ENST00000397032.8:c.1239C=	ENSP00000380226.3:p.Asp413=
ENST00000436370.7:c.1170C=	ENSP00000391890.2:p.Asp390=
ENST00000589598.5:n.87C=
ENST00000591968.1:n.434C=
ENST00000593085.1:n.1249C=
NM_000285.3:c.1362C=	NP_000276.2:p.Asp454=
NM_001166056.1:c.1239C=	NP_001159528.1:p.Asp413=
NM_001166057.1:c.1170C=	NP_001159529.1:p.Asp390=
NM_000285.4:c.1362C= MANE Select	NP_000276.2:p.Asp454=
NM_001166056.2:c.1239C=	NP_001159528.1:p.Asp413=
NM_001166057.2:c.1170C=	NP_001159529.1:p.Asp390=