Canonical Allele Identifier: CA2332698542

Gene: PEPD

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33387401A= , CM000681.2:g.33387401A=	GRCh38
NC_000019.9:g.33878307A= , CM000681.1:g.33878307A=	GRCh37
NC_000019.8:g.38570147A=	NCBI36
NG_013358.1:g.139493T=
NG_013358.2:g.139493T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.1491T=	ENSP00000468516.4:p.Ile497=
ENST00000651901.2:c.1515T=	ENSP00000498922.2:p.Ile505=
ENST00000698359.1:c.1380T=	ENSP00000513682.1:p.Ile460=
ENST00000698360.1:c.1476T=	ENSP00000513683.1:p.Ile492=
ENST00000698361.1:c.*53T=	ENSP00000513684.1:n.*53T=
ENST00000698362.1:c.*562T=	ENSP00000513685.1:n.*562T=
ENST00000698426.1:c.1104T=	ENSP00000513713.1:p.Ile368=
ENST00000698427.1:c.1467T=	ENSP00000513714.1:p.Ile489=
ENST00000698428.1:c.1104T=	ENSP00000513715.1:p.Ile368=
ENST00000698429.1:n.1308T=
ENST00000698430.1:c.1675T=
ENST00000698431.1:c.1162T=	ENSP00000513717.1:n.1162T=
ENST00000698432.1:c.1234T=
ENST00000698433.1:n.887T=
ENST00000244137.12:c.1425T= MANE Select	ENSP00000244137.5:p.Ile475=
ENST00000588328.6:c.1480T=
ENST00000651901.1:c.1511T=
ENST00000244137.11:c.1425T=	ENSP00000244137.5:p.Ile475=
ENST00000397032.8:c.1302T=	ENSP00000380226.3:p.Ile434=
ENST00000436370.7:c.1233T=	ENSP00000391890.2:p.Ile411=
ENST00000589598.5:n.150T=
ENST00000591968.1:n.497T=
ENST00000593085.1:n.1312T=
NM_000285.3:c.1425T=	NP_000276.2:p.Ile475=
NM_001166056.1:c.1302T=	NP_001159528.1:p.Ile434=
NM_001166057.1:c.1233T=	NP_001159529.1:p.Ile411=
NM_000285.4:c.1425T= MANE Select	NP_000276.2:p.Ile475=
NM_001166056.2:c.1302T=	NP_001159528.1:p.Ile434=
NM_001166057.2:c.1233T=	NP_001159529.1:p.Ile411=