Canonical Allele Identifier: CA2584321414

Gene: PEPD

Linked Data

• gnomAD v4: 19-33387298-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33387298G>T , CM000681.2:g.33387298G>T	GRCh38
NC_000019.9:g.33878204G>T , CM000681.1:g.33878204G>T	GRCh37
NC_000019.8:g.38570044G>T	NCBI36
NG_013358.1:g.139596C>A
NG_013358.2:g.139596C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.*46C>A	ENSP00000468516.4:n.*46C>A
ENST00000651901.2:c.*46C>A	ENSP00000498922.2:n.*46C>A
ENST00000698359.1:c.*46C>A	ENSP00000513682.1:n.*46C>A
ENST00000698360.1:c.*46C>A	ENSP00000513683.1:n.*46C>A
ENST00000698361.1:c.*156C>A	ENSP00000513684.1:n.*156C>A
ENST00000698362.1:c.*665C>A	ENSP00000513685.1:n.*665C>A
ENST00000698426.1:c.*46C>A	ENSP00000513713.1:n.*46C>A
ENST00000698427.1:c.*46C>A	ENSP00000513714.1:n.*46C>A
ENST00000698428.1:c.*46C>A	ENSP00000513715.1:n.*46C>A
ENST00000698429.1:n.1411C>A
ENST00000698430.1:c.1778C>A
ENST00000698431.1:c.1265C>A	ENSP00000513717.1:n.1265C>A
ENST00000698432.1:c.1337C>A
ENST00000244137.12:c.*46C>A MANE Select	ENSP00000244137.5:n.*46C>A
ENST00000588328.6:c.1583C>A
ENST00000651901.1:c.1614C>A
ENST00000244137.11:c.*46C>A	ENSP00000244137.5:n.*46C>A
ENST00000397032.8:c.*46C>A	ENSP00000380226.3:n.*46C>A
ENST00000436370.7:c.*46C>A	ENSP00000391890.2:n.*46C>A
ENST00000589598.5:n.253C>A
ENST00000591968.1:n.600C>A
ENST00000593085.1:n.1415C>A
NM_000285.3:c.*46C>A	NP_000276.2:n.*46C>A
NM_001166056.1:c.*46C>A	NP_001159528.1:n.*46C>A
NM_001166057.1:c.*46C>A	NP_001159529.1:n.*46C>A
NM_000285.4:c.*46C>A MANE Select	NP_000276.2:n.*46C>A
NM_001166056.2:c.*46C>A	NP_001159528.1:n.*46C>A
NM_001166057.2:c.*46C>A	NP_001159529.1:n.*46C>A