Canonical Allele Identifier: CA2332698553

Gene: PEPD

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33387419G= , CM000681.2:g.33387419G=	GRCh38
NC_000019.9:g.33878325G= , CM000681.1:g.33878325G=	GRCh37
NC_000019.8:g.38570165G=	NCBI36
NG_013358.1:g.139475C=
NG_013358.2:g.139475C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.1473C=	ENSP00000468516.4:p.Pro491=
ENST00000651901.2:c.1497C=	ENSP00000498922.2:p.Pro499=
ENST00000698359.1:c.1362C=	ENSP00000513682.1:p.Pro454=
ENST00000698360.1:c.1458C=	ENSP00000513683.1:p.Pro486=
ENST00000698361.1:c.*35C=	ENSP00000513684.1:n.*35C=
ENST00000698362.1:c.*544C=	ENSP00000513685.1:n.*544C=
ENST00000698426.1:c.1086C=	ENSP00000513713.1:p.Pro362=
ENST00000698427.1:c.1449C=	ENSP00000513714.1:p.Pro483=
ENST00000698428.1:c.1086C=	ENSP00000513715.1:p.Pro362=
ENST00000698429.1:n.1290C=
ENST00000698430.1:c.1657C=
ENST00000698431.1:c.1144C=	ENSP00000513717.1:n.1144C=
ENST00000698432.1:c.1216C=
ENST00000698433.1:n.869C=
ENST00000244137.12:c.1407C= MANE Select	ENSP00000244137.5:p.Pro469=
ENST00000588328.6:c.1462C=
ENST00000651901.1:c.1493C=
ENST00000244137.11:c.1407C=	ENSP00000244137.5:p.Pro469=
ENST00000397032.8:c.1284C=	ENSP00000380226.3:p.Pro428=
ENST00000436370.7:c.1215C=	ENSP00000391890.2:p.Pro405=
ENST00000589598.5:n.132C=
ENST00000591968.1:n.479C=
ENST00000593085.1:n.1294C=
NM_000285.3:c.1407C=	NP_000276.2:p.Pro469=
NM_001166056.1:c.1284C=	NP_001159528.1:p.Pro428=
NM_001166057.1:c.1215C=	NP_001159529.1:p.Pro405=
NM_000285.4:c.1407C= MANE Select	NP_000276.2:p.Pro469=
NM_001166056.2:c.1284C=	NP_001159528.1:p.Pro428=
NM_001166057.2:c.1215C=	NP_001159529.1:p.Pro405=