Canonical Allele Identifier: CA405219459

Gene: PEPD

Linked Data

• dbSNP Id: rs144944440
• MyVariant Identifiers: chr19:g.33878290C>T (hg19) ; chr19:g.33387384C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33387384C>T , CM000681.2:g.33387384C>T	GRCh38
NC_000019.9:g.33878290C>T , CM000681.1:g.33878290C>T	GRCh37
NC_000019.8:g.38570130C>T	NCBI36
NG_013358.1:g.139510G>A
NG_013358.2:g.139510G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.1508G>A	ENSP00000468516.4:p.Gly503Asp
ENST00000651901.2:c.1532G>A	ENSP00000498922.2:p.Gly511Asp
ENST00000698359.1:c.1397G>A	ENSP00000513682.1:p.Gly466Asp
ENST00000698360.1:c.1493G>A	ENSP00000513683.1:p.Gly498Asp
ENST00000698361.1:c.*70G>A	ENSP00000513684.1:n.*70G>A
ENST00000698362.1:c.*579G>A	ENSP00000513685.1:n.*579G>A
ENST00000698426.1:c.1121G>A	ENSP00000513713.1:p.Gly374Asp
ENST00000698427.1:c.1484G>A	ENSP00000513714.1:p.Gly495Asp
ENST00000698428.1:c.1121G>A	ENSP00000513715.1:p.Gly374Asp
ENST00000698429.1:n.1325G>A
ENST00000698430.1:c.1692G>A
ENST00000698431.1:c.1179G>A	ENSP00000513717.1:n.1179G>A
ENST00000698432.1:c.1251G>A
ENST00000698433.1:n.904G>A
ENST00000244137.12:c.1442G>A MANE Select	ENSP00000244137.5:p.Gly481Asp
ENST00000588328.6:c.1497G>A
ENST00000651901.1:c.1528G>A
ENST00000244137.11:c.1442G>A	ENSP00000244137.5:p.Gly481Asp
ENST00000397032.8:c.1319G>A	ENSP00000380226.3:p.Gly440Asp
ENST00000436370.7:c.1250G>A	ENSP00000391890.2:p.Gly417Asp
ENST00000589598.5:n.167G>A
ENST00000591968.1:n.514G>A
ENST00000593085.1:n.1329G>A
NM_000285.3:c.1442G>A	NP_000276.2:p.Gly481Asp
NM_001166056.1:c.1319G>A	NP_001159528.1:p.Gly440Asp
NM_001166057.1:c.1250G>A	NP_001159529.1:p.Gly417Asp
NM_000285.4:c.1442G>A MANE Select	NP_000276.2:p.Gly481Asp
NM_001166056.2:c.1319G>A	NP_001159528.1:p.Gly440Asp
NM_001166057.2:c.1250G>A	NP_001159529.1:p.Gly417Asp