Canonical Allele Identifier: CA2332698551

Gene: PEPD

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33387417C= , CM000681.2:g.33387417C=	GRCh38
NC_000019.9:g.33878323C= , CM000681.1:g.33878323C=	GRCh37
NC_000019.8:g.38570163C=	NCBI36
NG_013358.1:g.139477G=
NG_013358.2:g.139477G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.1475G=	ENSP00000468516.4:p.Arg492=
ENST00000651901.2:c.1499G=	ENSP00000498922.2:p.Arg500=
ENST00000698359.1:c.1364G=	ENSP00000513682.1:p.Arg455=
ENST00000698360.1:c.1460G=	ENSP00000513683.1:p.Arg487=
ENST00000698361.1:c.*37G=	ENSP00000513684.1:n.*37G=
ENST00000698362.1:c.*546G=	ENSP00000513685.1:n.*546G=
ENST00000698426.1:c.1088G=	ENSP00000513713.1:p.Arg363=
ENST00000698427.1:c.1451G=	ENSP00000513714.1:p.Arg484=
ENST00000698428.1:c.1088G=	ENSP00000513715.1:p.Arg363=
ENST00000698429.1:n.1292G=
ENST00000698430.1:c.1659G=
ENST00000698431.1:c.1146G=	ENSP00000513717.1:n.1146G=
ENST00000698432.1:c.1218G=
ENST00000698433.1:n.871G=
ENST00000244137.12:c.1409G= MANE Select	ENSP00000244137.5:p.Arg470=
ENST00000588328.6:c.1464G=
ENST00000651901.1:c.1495G=
ENST00000244137.11:c.1409G=	ENSP00000244137.5:p.Arg470=
ENST00000397032.8:c.1286G=	ENSP00000380226.3:p.Arg429=
ENST00000436370.7:c.1217G=	ENSP00000391890.2:p.Arg406=
ENST00000589598.5:n.134G=
ENST00000591968.1:n.481G=
ENST00000593085.1:n.1296G=
NM_000285.3:c.1409G=	NP_000276.2:p.Arg470=
NM_001166056.1:c.1286G=	NP_001159528.1:p.Arg429=
NM_001166057.1:c.1217G=	NP_001159529.1:p.Arg406=
NM_000285.4:c.1409G= MANE Select	NP_000276.2:p.Arg470=
NM_001166056.2:c.1286G=	NP_001159528.1:p.Arg429=
NM_001166057.2:c.1217G=	NP_001159529.1:p.Arg406=