Canonical Allele Identifier: CA2332698538

Gene: PEPD

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33387391T= , CM000681.2:g.33387391T=	GRCh38
NC_000019.9:g.33878297T= , CM000681.1:g.33878297T=	GRCh37
NC_000019.8:g.38570137T=	NCBI36
NG_013358.1:g.139503A=
NG_013358.2:g.139503A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.1501A=	ENSP00000468516.4:p.Met501=
ENST00000651901.2:c.1525A=	ENSP00000498922.2:p.Met509=
ENST00000698359.1:c.1390A=	ENSP00000513682.1:p.Met464=
ENST00000698360.1:c.1486A=	ENSP00000513683.1:p.Met496=
ENST00000698361.1:c.*63A=	ENSP00000513684.1:n.*63A=
ENST00000698362.1:c.*572A=	ENSP00000513685.1:n.*572A=
ENST00000698426.1:c.1114A=	ENSP00000513713.1:p.Met372=
ENST00000698427.1:c.1477A=	ENSP00000513714.1:p.Met493=
ENST00000698428.1:c.1114A=	ENSP00000513715.1:p.Met372=
ENST00000698429.1:n.1318A=
ENST00000698430.1:c.1685A=
ENST00000698431.1:c.1172A=	ENSP00000513717.1:n.1172A=
ENST00000698432.1:c.1244A=
ENST00000698433.1:n.897A=
ENST00000244137.12:c.1435A= MANE Select	ENSP00000244137.5:p.Met479=
ENST00000588328.6:c.1490A=
ENST00000651901.1:c.1521A=
ENST00000244137.11:c.1435A=	ENSP00000244137.5:p.Met479=
ENST00000397032.8:c.1312A=	ENSP00000380226.3:p.Met438=
ENST00000436370.7:c.1243A=	ENSP00000391890.2:p.Met415=
ENST00000589598.5:n.160A=
ENST00000591968.1:n.507A=
ENST00000593085.1:n.1322A=
NM_000285.3:c.1435A=	NP_000276.2:p.Met479=
NM_001166056.1:c.1312A=	NP_001159528.1:p.Met438=
NM_001166057.1:c.1243A=	NP_001159529.1:p.Met415=
NM_000285.4:c.1435A= MANE Select	NP_000276.2:p.Met479=
NM_001166056.2:c.1312A=	NP_001159528.1:p.Met438=
NM_001166057.2:c.1243A=	NP_001159529.1:p.Met415=