Canonical Allele Identifier: CA506686781

Gene: PEPD

Linked Data

• MyVariant Identifiers: chr19:g.33878334G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33387428G>T , CM000681.2:g.33387428G>T	GRCh38
NC_000019.9:g.33878334G>T , CM000681.1:g.33878334G>T	GRCh37
NC_000019.8:g.38570174G>T	NCBI36
NG_013358.1:g.139466C>A
NG_013358.2:g.139466C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.1464C>A	ENSP00000468516.4:p.Thr488=
ENST00000651901.2:c.1488C>A	ENSP00000498922.2:p.Thr496=
ENST00000698359.1:c.1353C>A	ENSP00000513682.1:p.Thr451=
ENST00000698360.1:c.1449C>A	ENSP00000513683.1:p.Thr483=
ENST00000698361.1:c.*26C>A	ENSP00000513684.1:n.*26C>A
ENST00000698362.1:c.*535C>A	ENSP00000513685.1:n.*535C>A
ENST00000698426.1:c.1077C>A	ENSP00000513713.1:p.Thr359=
ENST00000698427.1:c.1440C>A	ENSP00000513714.1:p.Thr480=
ENST00000698428.1:c.1077C>A	ENSP00000513715.1:p.Thr359=
ENST00000698429.1:n.1281C>A
ENST00000698430.1:c.1648C>A
ENST00000698431.1:c.1135C>A	ENSP00000513717.1:n.1135C>A
ENST00000698432.1:c.1207C>A
ENST00000698433.1:n.860C>A
ENST00000244137.12:c.1398C>A MANE Select	ENSP00000244137.5:p.Thr466=
ENST00000588328.6:c.1453C>A
ENST00000651901.1:c.1484C>A
ENST00000244137.11:c.1398C>A	ENSP00000244137.5:p.Thr466=
ENST00000397032.8:c.1275C>A	ENSP00000380226.3:p.Thr425=
ENST00000436370.7:c.1206C>A	ENSP00000391890.2:p.Thr402=
ENST00000589598.5:n.123C>A
ENST00000591968.1:n.470C>A
ENST00000593085.1:n.1285C>A
NM_000285.3:c.1398C>A	NP_000276.2:p.Thr466=
NM_001166056.1:c.1275C>A	NP_001159528.1:p.Thr425=
NM_001166057.1:c.1206C>A	NP_001159529.1:p.Thr402=
NM_000285.4:c.1398C>A MANE Select	NP_000276.2:p.Thr466=
NM_001166056.2:c.1275C>A	NP_001159528.1:p.Thr425=
NM_001166057.2:c.1206C>A	NP_001159529.1:p.Thr402=