Canonical Allele Identifier: CA2332698557

Gene: PEPD

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33387426C= , CM000681.2:g.33387426C=	GRCh38
NC_000019.9:g.33878332C= , CM000681.1:g.33878332C=	GRCh37
NC_000019.8:g.38570172C=	NCBI36
NG_013358.1:g.139468G=
NG_013358.2:g.139468G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.1466G=	ENSP00000468516.4:p.Cys489=
ENST00000651901.2:c.1490G=	ENSP00000498922.2:p.Cys497=
ENST00000698359.1:c.1355G=	ENSP00000513682.1:p.Cys452=
ENST00000698360.1:c.1451G=	ENSP00000513683.1:p.Cys484=
ENST00000698361.1:c.*28G=	ENSP00000513684.1:n.*28G=
ENST00000698362.1:c.*537G=	ENSP00000513685.1:n.*537G=
ENST00000698426.1:c.1079G=	ENSP00000513713.1:p.Cys360=
ENST00000698427.1:c.1442G=	ENSP00000513714.1:p.Cys481=
ENST00000698428.1:c.1079G=	ENSP00000513715.1:p.Cys360=
ENST00000698429.1:n.1283G=
ENST00000698430.1:c.1650G=
ENST00000698431.1:c.1137G=	ENSP00000513717.1:n.1137G=
ENST00000698432.1:c.1209G=
ENST00000698433.1:n.862G=
ENST00000244137.12:c.1400G= MANE Select	ENSP00000244137.5:p.Cys467=
ENST00000588328.6:c.1455G=
ENST00000651901.1:c.1486G=
ENST00000244137.11:c.1400G=	ENSP00000244137.5:p.Cys467=
ENST00000397032.8:c.1277G=	ENSP00000380226.3:p.Cys426=
ENST00000436370.7:c.1208G=	ENSP00000391890.2:p.Cys403=
ENST00000589598.5:n.125G=
ENST00000591968.1:n.472G=
ENST00000593085.1:n.1287G=
NM_000285.3:c.1400G=	NP_000276.2:p.Cys467=
NM_001166056.1:c.1277G=	NP_001159528.1:p.Cys426=
NM_001166057.1:c.1208G=	NP_001159529.1:p.Cys403=
NM_000285.4:c.1400G= MANE Select	NP_000276.2:p.Cys467=
NM_001166056.2:c.1277G=	NP_001159528.1:p.Cys426=
NM_001166057.2:c.1208G=	NP_001159529.1:p.Cys403=