Canonical Allele Identifier: CA2332698566

Gene: PEPD

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33387453G= , CM000681.2:g.33387453G=	GRCh38
NC_000019.9:g.33878359G= , CM000681.1:g.33878359G=	GRCh37
NC_000019.8:g.38570199G=	NCBI36
NG_013358.1:g.139441C=
NG_013358.2:g.139441C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.1439C=	ENSP00000468516.4:p.Thr480=
ENST00000651901.2:c.1463C=	ENSP00000498922.2:p.Thr488=
ENST00000698359.1:c.1328C=	ENSP00000513682.1:p.Thr443=
ENST00000698360.1:c.1424C=	ENSP00000513683.1:p.Thr475=
ENST00000698361.1:c.*1C=	ENSP00000513684.1:n.*1C=
ENST00000698362.1:c.*510C=	ENSP00000513685.1:n.*510C=
ENST00000698426.1:c.1052C=	ENSP00000513713.1:p.Thr351=
ENST00000698427.1:c.1415C=	ENSP00000513714.1:p.Thr472=
ENST00000698428.1:c.1052C=	ENSP00000513715.1:p.Thr351=
ENST00000698429.1:n.1256C=
ENST00000698430.1:c.1623C=
ENST00000698431.1:c.1110C=	ENSP00000513717.1:n.1110C=
ENST00000698432.1:c.1182C=
ENST00000698433.1:n.835C=
ENST00000244137.12:c.1373C= MANE Select	ENSP00000244137.5:p.Thr458=
ENST00000588328.6:c.1428C=
ENST00000651901.1:c.1459C=
ENST00000244137.11:c.1373C=	ENSP00000244137.5:p.Thr458=
ENST00000397032.8:c.1250C=	ENSP00000380226.3:p.Thr417=
ENST00000436370.7:c.1181C=	ENSP00000391890.2:p.Thr394=
ENST00000589598.5:n.98C=
ENST00000591968.1:n.445C=
ENST00000593085.1:n.1260C=
NM_000285.3:c.1373C=	NP_000276.2:p.Thr458=
NM_001166056.1:c.1250C=	NP_001159528.1:p.Thr417=
NM_001166057.1:c.1181C=	NP_001159529.1:p.Thr394=
NM_000285.4:c.1373C= MANE Select	NP_000276.2:p.Thr458=
NM_001166056.2:c.1250C=	NP_001159528.1:p.Thr417=
NM_001166057.2:c.1181C=	NP_001159529.1:p.Thr394=