Canonical Allele Identifier: CA2332698630

Gene: PEPD

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33387550A= , CM000681.2:g.33387550A=	GRCh38
NC_000019.9:g.33878456A= , CM000681.1:g.33878456A=	GRCh37
NC_000019.8:g.38570296A=	NCBI36
NG_013358.1:g.139344T=
NG_013358.2:g.139344T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.1411-69T=	ENSP00000468516.4:n.1411-69T=
ENST00000651901.2:c.1435-69T=	ENSP00000498922.2:n.1435-69T=
ENST00000698359.1:c.1300-69T=	ENSP00000513682.1:n.1300-69T=
ENST00000698360.1:c.1396-69T=	ENSP00000513683.1:n.1396-69T=
ENST00000698361.1:c.1461-69T=	ENSP00000513684.1:n.1461-69T=
ENST00000698362.1:c.*413T=	ENSP00000513685.1:n.*413T=
ENST00000698426.1:c.1024-69T=	ENSP00000513713.1:n.1024-69T=
ENST00000698427.1:c.1387-69T=	ENSP00000513714.1:n.1387-69T=
ENST00000698428.1:c.1024-69T=	ENSP00000513715.1:n.1024-69T=
ENST00000698429.1:n.1228-69T=
ENST00000698430.1:c.1595-69T=
ENST00000698431.1:c.1082-69T=	ENSP00000513717.1:n.1082-69T=
ENST00000698432.1:c.1154-69T=
ENST00000698433.1:n.807-69T=
ENST00000244137.12:c.1345-69T= MANE Select	ENSP00000244137.5:n.1345-69T=
ENST00000588328.6:c.1400-69T=
ENST00000651901.1:c.1431-69T=
ENST00000244137.11:c.1345-69T=	ENSP00000244137.5:n.1345-69T=
ENST00000397032.8:c.1222-69T=	ENSP00000380226.3:n.1222-69T=
ENST00000436370.7:c.1153-69T=	ENSP00000391890.2:n.1153-69T=
ENST00000589598.5:n.70-69T=
ENST00000591968.1:n.417-69T=
ENST00000593085.1:n.1232-69T=
NM_000285.3:c.1345-69T=	NP_000276.2:n.1345-69T=
NM_001166056.1:c.1222-69T=	NP_001159528.1:n.1222-69T=
NM_001166057.1:c.1153-69T=	NP_001159529.1:n.1153-69T=
NM_000285.4:c.1345-69T= MANE Select	NP_000276.2:n.1345-69T=
NM_001166056.2:c.1222-69T=	NP_001159528.1:n.1222-69T=
NM_001166057.2:c.1153-69T=	NP_001159529.1:n.1153-69T=