Canonical Allele Identifier: CA2332698563

Gene: PEPD

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33387445C= , CM000681.2:g.33387445C=	GRCh38
NC_000019.9:g.33878351C= , CM000681.1:g.33878351C=	GRCh37
NC_000019.8:g.38570191C=	NCBI36
NG_013358.1:g.139449G=
NG_013358.2:g.139449G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.1447G=	ENSP00000468516.4:p.Gly483=
ENST00000651901.2:c.1471G=	ENSP00000498922.2:p.Gly491=
ENST00000698359.1:c.1336G=	ENSP00000513682.1:p.Gly446=
ENST00000698360.1:c.1432G=	ENSP00000513683.1:p.Gly478=
ENST00000698361.1:c.*9G=	ENSP00000513684.1:n.*9G=
ENST00000698362.1:c.*518G=	ENSP00000513685.1:n.*518G=
ENST00000698426.1:c.1060G=	ENSP00000513713.1:p.Gly354=
ENST00000698427.1:c.1423G=	ENSP00000513714.1:p.Gly475=
ENST00000698428.1:c.1060G=	ENSP00000513715.1:p.Gly354=
ENST00000698429.1:n.1264G=
ENST00000698430.1:c.1631G=
ENST00000698431.1:c.1118G=	ENSP00000513717.1:n.1118G=
ENST00000698432.1:c.1190G=
ENST00000698433.1:n.843G=
ENST00000244137.12:c.1381G= MANE Select	ENSP00000244137.5:p.Gly461=
ENST00000588328.6:c.1436G=
ENST00000651901.1:c.1467G=
ENST00000244137.11:c.1381G=	ENSP00000244137.5:p.Gly461=
ENST00000397032.8:c.1258G=	ENSP00000380226.3:p.Gly420=
ENST00000436370.7:c.1189G=	ENSP00000391890.2:p.Gly397=
ENST00000589598.5:n.106G=
ENST00000591968.1:n.453G=
ENST00000593085.1:n.1268G=
NM_000285.3:c.1381G=	NP_000276.2:p.Gly461=
NM_001166056.1:c.1258G=	NP_001159528.1:p.Gly420=
NM_001166057.1:c.1189G=	NP_001159529.1:p.Gly397=
NM_000285.4:c.1381G= MANE Select	NP_000276.2:p.Gly461=
NM_001166056.2:c.1258G=	NP_001159528.1:p.Gly420=
NM_001166057.2:c.1189G=	NP_001159529.1:p.Gly397=