Canonical Allele Identifier: CA405219451

Gene: PEPD

Linked Data

• MyVariant Identifiers: chr19:g.33878288A>T (hg19) ; chr19:g.33387382A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33387382A>T , CM000681.2:g.33387382A>T	GRCh38
NC_000019.9:g.33878288A>T , CM000681.1:g.33878288A>T	GRCh37
NC_000019.8:g.38570128A>T	NCBI36
NG_013358.1:g.139512T>A
NG_013358.2:g.139512T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.1510T>A	ENSP00000468516.4:p.Cys504Ser
ENST00000651901.2:c.1534T>A	ENSP00000498922.2:p.Cys512Ser
ENST00000698359.1:c.1399T>A	ENSP00000513682.1:p.Cys467Ser
ENST00000698360.1:c.1495T>A	ENSP00000513683.1:p.Cys499Ser
ENST00000698361.1:c.*72T>A	ENSP00000513684.1:n.*72T>A
ENST00000698362.1:c.*581T>A	ENSP00000513685.1:n.*581T>A
ENST00000698426.1:c.1123T>A	ENSP00000513713.1:p.Cys375Ser
ENST00000698427.1:c.1486T>A	ENSP00000513714.1:p.Cys496Ser
ENST00000698428.1:c.1123T>A	ENSP00000513715.1:p.Cys375Ser
ENST00000698429.1:n.1327T>A
ENST00000698430.1:c.1694T>A
ENST00000698431.1:c.1181T>A	ENSP00000513717.1:n.1181T>A
ENST00000698432.1:c.1253T>A
ENST00000698433.1:n.906T>A
ENST00000244137.12:c.1444T>A MANE Select	ENSP00000244137.5:p.Cys482Ser
ENST00000588328.6:c.1499T>A
ENST00000651901.1:c.1530T>A
ENST00000244137.11:c.1444T>A	ENSP00000244137.5:p.Cys482Ser
ENST00000397032.8:c.1321T>A	ENSP00000380226.3:p.Cys441Ser
ENST00000436370.7:c.1252T>A	ENSP00000391890.2:p.Cys418Ser
ENST00000589598.5:n.169T>A
ENST00000591968.1:n.516T>A
ENST00000593085.1:n.1331T>A
NM_000285.3:c.1444T>A	NP_000276.2:p.Cys482Ser
NM_001166056.1:c.1321T>A	NP_001159528.1:p.Cys441Ser
NM_001166057.1:c.1252T>A	NP_001159529.1:p.Cys418Ser
NM_000285.4:c.1444T>A MANE Select	NP_000276.2:p.Cys482Ser
NM_001166056.2:c.1321T>A	NP_001159528.1:p.Cys441Ser
NM_001166057.2:c.1252T>A	NP_001159529.1:p.Cys418Ser