Canonical Allele Identifier: CA405219734

Gene: PEPD

Linked Data

• dbSNP Id: rs772139535
• MyVariant Identifiers: chr19:g.33878370G>C (hg19) ; chr19:g.33387464G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33387464G>C , CM000681.2:g.33387464G>C	GRCh38
NC_000019.9:g.33878370G>C , CM000681.1:g.33878370G>C	GRCh37
NC_000019.8:g.38570210G>C	NCBI36
NG_013358.1:g.139430C>G
NG_013358.2:g.139430C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.1428C>G	ENSP00000468516.4:p.Asp476Glu
ENST00000651901.2:c.1452C>G	ENSP00000498922.2:p.Asp484Glu
ENST00000698359.1:c.1317C>G	ENSP00000513682.1:p.Asp439Glu
ENST00000698360.1:c.1413C>G	ENSP00000513683.1:p.Asp471Glu
ENST00000698361.1:c.1478C>G	ENSP00000513684.1:p.Thr493Arg
ENST00000698362.1:c.*499C>G	ENSP00000513685.1:n.*499C>G
ENST00000698426.1:c.1041C>G	ENSP00000513713.1:p.Asp347Glu
ENST00000698427.1:c.1404C>G	ENSP00000513714.1:p.Asp468Glu
ENST00000698428.1:c.1041C>G	ENSP00000513715.1:p.Asp347Glu
ENST00000698429.1:n.1245C>G
ENST00000698430.1:c.1612C>G
ENST00000698431.1:c.1099C>G	ENSP00000513717.1:n.1099C>G
ENST00000698432.1:c.1171C>G
ENST00000698433.1:n.824C>G
ENST00000244137.12:c.1362C>G MANE Select	ENSP00000244137.5:p.Asp454Glu
ENST00000588328.6:c.1417C>G
ENST00000651901.1:c.1448C>G
ENST00000244137.11:c.1362C>G	ENSP00000244137.5:p.Asp454Glu
ENST00000397032.8:c.1239C>G	ENSP00000380226.3:p.Asp413Glu
ENST00000436370.7:c.1170C>G	ENSP00000391890.2:p.Asp390Glu
ENST00000589598.5:n.87C>G
ENST00000591968.1:n.434C>G
ENST00000593085.1:n.1249C>G
NM_000285.3:c.1362C>G	NP_000276.2:p.Asp454Glu
NM_001166056.1:c.1239C>G	NP_001159528.1:p.Asp413Glu
NM_001166057.1:c.1170C>G	NP_001159529.1:p.Asp390Glu
NM_000285.4:c.1362C>G MANE Select	NP_000276.2:p.Asp454Glu
NM_001166056.2:c.1239C>G	NP_001159528.1:p.Asp413Glu
NM_001166057.2:c.1170C>G	NP_001159529.1:p.Asp390Glu