Canonical Allele Identifier: CA2332763099

Gene: PEPD

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33521746G= , CM000681.2:g.33521746G=	GRCh38
NC_000019.9:g.34012652G= , CM000681.1:g.34012652G=	GRCh37
NC_000019.8:g.38704492G=	NCBI36
NG_013358.1:g.5148C=
NG_013358.2:g.5148C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.15C=	ENSP00000468516.4:p.Thr5=
ENST00000651646.2:c.15C=	ENSP00000498950.2:p.Thr5=
ENST00000651901.2:c.15C=	ENSP00000498922.2:p.Thr5=
ENST00000698359.1:c.15C=	ENSP00000513682.1:p.Thr5=
ENST00000698360.1:c.15C=	ENSP00000513683.1:p.Thr5=
ENST00000698361.1:c.15C=	ENSP00000513684.1:p.Thr5=
ENST00000698362.1:c.15C=	ENSP00000513685.1:p.Thr5=
ENST00000698363.1:n.78C=
ENST00000698364.1:n.78C=
ENST00000698365.1:n.78C=
ENST00000698426.1:c.-501C=	ENSP00000513713.1:n.-501C=
ENST00000698427.1:c.-51C=	ENSP00000513714.1:n.-51C=
ENST00000698428.1:c.-379C=	ENSP00000513715.1:n.-379C=
ENST00000698435.1:c.15C=	ENSP00000513719.1:p.Thr5=
ENST00000698436.1:c.15C=	ENSP00000513720.1:p.Thr5=
ENST00000244137.12:c.15C= MANE Select	ENSP00000244137.5:p.Thr5=
ENST00000588328.6:c.4C=
ENST00000651646.1:c.13C=
ENST00000651901.1:c.11C=
ENST00000244137.11:c.15C=	ENSP00000244137.5:p.Thr5=
ENST00000397032.8:c.15C=	ENSP00000380226.3:p.Thr5=
ENST00000436370.7:c.15C=	ENSP00000391890.2:p.Thr5=
NM_000285.3:c.15C=	NP_000276.2:p.Thr5=
NM_001166056.1:c.15C=	NP_001159528.1:p.Thr5=
NM_001166057.1:c.15C=	NP_001159529.1:p.Thr5=
NM_000285.4:c.15C= MANE Select	NP_000276.2:p.Thr5=
NM_001166056.2:c.15C=	NP_001159528.1:p.Thr5=
NM_001166057.2:c.15C=	NP_001159529.1:p.Thr5=