Canonical Allele Identifier: CA2332698549

Gene: PEPD

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33387414G= , CM000681.2:g.33387414G=	GRCh38
NC_000019.9:g.33878320G= , CM000681.1:g.33878320G=	GRCh37
NC_000019.8:g.38570160G=	NCBI36
NG_013358.1:g.139480C=
NG_013358.2:g.139480C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.1478C=	ENSP00000468516.4:p.Thr493=
ENST00000651901.2:c.1502C=	ENSP00000498922.2:p.Thr501=
ENST00000698359.1:c.1367C=	ENSP00000513682.1:p.Thr456=
ENST00000698360.1:c.1463C=	ENSP00000513683.1:p.Thr488=
ENST00000698361.1:c.*40C=	ENSP00000513684.1:n.*40C=
ENST00000698362.1:c.*549C=	ENSP00000513685.1:n.*549C=
ENST00000698426.1:c.1091C=	ENSP00000513713.1:p.Thr364=
ENST00000698427.1:c.1454C=	ENSP00000513714.1:p.Thr485=
ENST00000698428.1:c.1091C=	ENSP00000513715.1:p.Thr364=
ENST00000698429.1:n.1295C=
ENST00000698430.1:c.1662C=
ENST00000698431.1:c.1149C=	ENSP00000513717.1:n.1149C=
ENST00000698432.1:c.1221C=
ENST00000698433.1:n.874C=
ENST00000244137.12:c.1412C= MANE Select	ENSP00000244137.5:p.Thr471=
ENST00000588328.6:c.1467C=
ENST00000651901.1:c.1498C=
ENST00000244137.11:c.1412C=	ENSP00000244137.5:p.Thr471=
ENST00000397032.8:c.1289C=	ENSP00000380226.3:p.Thr430=
ENST00000436370.7:c.1220C=	ENSP00000391890.2:p.Thr407=
ENST00000589598.5:n.137C=
ENST00000591968.1:n.484C=
ENST00000593085.1:n.1299C=
NM_000285.3:c.1412C=	NP_000276.2:p.Thr471=
NM_001166056.1:c.1289C=	NP_001159528.1:p.Thr430=
NM_001166057.1:c.1220C=	NP_001159529.1:p.Thr407=
NM_000285.4:c.1412C= MANE Select	NP_000276.2:p.Thr471=
NM_001166056.2:c.1289C=	NP_001159528.1:p.Thr430=
NM_001166057.2:c.1220C=	NP_001159529.1:p.Thr407=