Canonical Allele Identifier: CA2332698541

Gene: PEPD

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33387395T= , CM000681.2:g.33387395T=	GRCh38
NC_000019.9:g.33878301T= , CM000681.1:g.33878301T=	GRCh37
NC_000019.8:g.38570141T=	NCBI36
NG_013358.1:g.139499A=
NG_013358.2:g.139499A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.1497A=	ENSP00000468516.4:p.Ala499=
ENST00000651901.2:c.1521A=	ENSP00000498922.2:p.Ala507=
ENST00000698359.1:c.1386A=	ENSP00000513682.1:p.Ala462=
ENST00000698360.1:c.1482A=	ENSP00000513683.1:p.Ala494=
ENST00000698361.1:c.*59A=	ENSP00000513684.1:n.*59A=
ENST00000698362.1:c.*568A=	ENSP00000513685.1:n.*568A=
ENST00000698426.1:c.1110A=	ENSP00000513713.1:p.Ala370=
ENST00000698427.1:c.1473A=	ENSP00000513714.1:p.Ala491=
ENST00000698428.1:c.1110A=	ENSP00000513715.1:p.Ala370=
ENST00000698429.1:n.1314A=
ENST00000698430.1:c.1681A=
ENST00000698431.1:c.1168A=	ENSP00000513717.1:n.1168A=
ENST00000698432.1:c.1240A=
ENST00000698433.1:n.893A=
ENST00000244137.12:c.1431A= MANE Select	ENSP00000244137.5:p.Ala477=
ENST00000588328.6:c.1486A=
ENST00000651901.1:c.1517A=
ENST00000244137.11:c.1431A=	ENSP00000244137.5:p.Ala477=
ENST00000397032.8:c.1308A=	ENSP00000380226.3:p.Ala436=
ENST00000436370.7:c.1239A=	ENSP00000391890.2:p.Ala413=
ENST00000589598.5:n.156A=
ENST00000591968.1:n.503A=
ENST00000593085.1:n.1318A=
NM_000285.3:c.1431A=	NP_000276.2:p.Ala477=
NM_001166056.1:c.1308A=	NP_001159528.1:p.Ala436=
NM_001166057.1:c.1239A=	NP_001159529.1:p.Ala413=
NM_000285.4:c.1431A= MANE Select	NP_000276.2:p.Ala477=
NM_001166056.2:c.1308A=	NP_001159528.1:p.Ala436=
NM_001166057.2:c.1239A=	NP_001159529.1:p.Ala413=