Canonical Allele Identifier: CA506686756

Gene: PEPD

Linked Data

• gnomAD v4: 19-33387392-G-A
• MyVariant Identifiers: chr19:g.33878298G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33387392G>A , CM000681.2:g.33387392G>A	GRCh38
NC_000019.9:g.33878298G>A , CM000681.1:g.33878298G>A	GRCh37
NC_000019.8:g.38570138G>A	NCBI36
NG_013358.1:g.139502C>T
NG_013358.2:g.139502C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.1500C>T	ENSP00000468516.4:p.Cys500=
ENST00000651901.2:c.1524C>T	ENSP00000498922.2:p.Cys508=
ENST00000698359.1:c.1389C>T	ENSP00000513682.1:p.Cys463=
ENST00000698360.1:c.1485C>T	ENSP00000513683.1:p.Cys495=
ENST00000698361.1:c.*62C>T	ENSP00000513684.1:n.*62C>T
ENST00000698362.1:c.*571C>T	ENSP00000513685.1:n.*571C>T
ENST00000698426.1:c.1113C>T	ENSP00000513713.1:p.Cys371=
ENST00000698427.1:c.1476C>T	ENSP00000513714.1:p.Cys492=
ENST00000698428.1:c.1113C>T	ENSP00000513715.1:p.Cys371=
ENST00000698429.1:n.1317C>T
ENST00000698430.1:c.1684C>T
ENST00000698431.1:c.1171C>T	ENSP00000513717.1:n.1171C>T
ENST00000698432.1:c.1243C>T
ENST00000698433.1:n.896C>T
ENST00000244137.12:c.1434C>T MANE Select	ENSP00000244137.5:p.Cys478=
ENST00000588328.6:c.1489C>T
ENST00000651901.1:c.1520C>T
ENST00000244137.11:c.1434C>T	ENSP00000244137.5:p.Cys478=
ENST00000397032.8:c.1311C>T	ENSP00000380226.3:p.Cys437=
ENST00000436370.7:c.1242C>T	ENSP00000391890.2:p.Cys414=
ENST00000589598.5:n.159C>T
ENST00000591968.1:n.506C>T
ENST00000593085.1:n.1321C>T
NM_000285.3:c.1434C>T	NP_000276.2:p.Cys478=
NM_001166056.1:c.1311C>T	NP_001159528.1:p.Cys437=
NM_001166057.1:c.1242C>T	NP_001159529.1:p.Cys414=
NM_000285.4:c.1434C>T MANE Select	NP_000276.2:p.Cys478=
NM_001166056.2:c.1311C>T	NP_001159528.1:p.Cys437=
NM_001166057.2:c.1242C>T	NP_001159529.1:p.Cys414=