Canonical Allele Identifier: CA506686769

Gene: PEPD

Linked Data

• MyVariant Identifiers: chr19:g.33878319A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33387413A>T , CM000681.2:g.33387413A>T	GRCh38
NC_000019.9:g.33878319A>T , CM000681.1:g.33878319A>T	GRCh37
NC_000019.8:g.38570159A>T	NCBI36
NG_013358.1:g.139481T>A
NG_013358.2:g.139481T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.1479T>A	ENSP00000468516.4:p.Thr493=
ENST00000651901.2:c.1503T>A	ENSP00000498922.2:p.Thr501=
ENST00000698359.1:c.1368T>A	ENSP00000513682.1:p.Thr456=
ENST00000698360.1:c.1464T>A	ENSP00000513683.1:p.Thr488=
ENST00000698361.1:c.*41T>A	ENSP00000513684.1:n.*41T>A
ENST00000698362.1:c.*550T>A	ENSP00000513685.1:n.*550T>A
ENST00000698426.1:c.1092T>A	ENSP00000513713.1:p.Thr364=
ENST00000698427.1:c.1455T>A	ENSP00000513714.1:p.Thr485=
ENST00000698428.1:c.1092T>A	ENSP00000513715.1:p.Thr364=
ENST00000698429.1:n.1296T>A
ENST00000698430.1:c.1663T>A
ENST00000698431.1:c.1150T>A	ENSP00000513717.1:n.1150T>A
ENST00000698432.1:c.1222T>A
ENST00000698433.1:n.875T>A
ENST00000244137.12:c.1413T>A MANE Select	ENSP00000244137.5:p.Thr471=
ENST00000588328.6:c.1468T>A
ENST00000651901.1:c.1499T>A
ENST00000244137.11:c.1413T>A	ENSP00000244137.5:p.Thr471=
ENST00000397032.8:c.1290T>A	ENSP00000380226.3:p.Thr430=
ENST00000436370.7:c.1221T>A	ENSP00000391890.2:p.Thr407=
ENST00000589598.5:n.138T>A
ENST00000591968.1:n.485T>A
ENST00000593085.1:n.1300T>A
NM_000285.3:c.1413T>A	NP_000276.2:p.Thr471=
NM_001166056.1:c.1290T>A	NP_001159528.1:p.Thr430=
NM_001166057.1:c.1221T>A	NP_001159529.1:p.Thr407=
NM_000285.4:c.1413T>A MANE Select	NP_000276.2:p.Thr471=
NM_001166056.2:c.1290T>A	NP_001159528.1:p.Thr430=
NM_001166057.2:c.1221T>A	NP_001159529.1:p.Thr407=