Canonical Allele Identifier: CA2332698534

Gene: PEPD

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33387380A= , CM000681.2:g.33387380A=	GRCh38
NC_000019.9:g.33878286A= , CM000681.1:g.33878286A=	GRCh37
NC_000019.8:g.38570126A=	NCBI36
NG_013358.1:g.139514T=
NG_013358.2:g.139514T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.1512T=	ENSP00000468516.4:p.Cys504=
ENST00000651901.2:c.1536T=	ENSP00000498922.2:p.Cys512=
ENST00000698359.1:c.1401T=	ENSP00000513682.1:p.Cys467=
ENST00000698360.1:c.1497T=	ENSP00000513683.1:p.Cys499=
ENST00000698361.1:c.*74T=	ENSP00000513684.1:n.*74T=
ENST00000698362.1:c.*583T=	ENSP00000513685.1:n.*583T=
ENST00000698426.1:c.1125T=	ENSP00000513713.1:p.Cys375=
ENST00000698427.1:c.1488T=	ENSP00000513714.1:p.Cys496=
ENST00000698428.1:c.1125T=	ENSP00000513715.1:p.Cys375=
ENST00000698429.1:n.1329T=
ENST00000698430.1:c.1696T=
ENST00000698431.1:c.1183T=	ENSP00000513717.1:n.1183T=
ENST00000698432.1:c.1255T=
ENST00000698433.1:n.908T=
ENST00000244137.12:c.1446T= MANE Select	ENSP00000244137.5:p.Cys482=
ENST00000588328.6:c.1501T=
ENST00000651901.1:c.1532T=
ENST00000244137.11:c.1446T=	ENSP00000244137.5:p.Cys482=
ENST00000397032.8:c.1323T=	ENSP00000380226.3:p.Cys441=
ENST00000436370.7:c.1254T=	ENSP00000391890.2:p.Cys418=
ENST00000589598.5:n.171T=
ENST00000591968.1:n.518T=
ENST00000593085.1:n.1333T=
NM_000285.3:c.1446T=	NP_000276.2:p.Cys482=
NM_001166056.1:c.1323T=	NP_001159528.1:p.Cys441=
NM_001166057.1:c.1254T=	NP_001159529.1:p.Cys418=
NM_000285.4:c.1446T= MANE Select	NP_000276.2:p.Cys482=
NM_001166056.2:c.1323T=	NP_001159528.1:p.Cys441=
NM_001166057.2:c.1254T=	NP_001159529.1:p.Cys418=