Canonical Allele Identifier: CA9363842

Gene: PEPD

Linked Data

• dbSNP Id: rs767382813
• ExAC: 19:33878225 G / A
• gnomAD v2: 19-33878225-G-A
• MyVariant Identifiers: chr19:g.33878225G>A (hg19) ; chr19:g.33387319G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33387319G>A , CM000681.2:g.33387319G>A	GRCh38
NC_000019.9:g.33878225G>A , CM000681.1:g.33878225G>A	GRCh37
NC_000019.8:g.38570065G>A	NCBI36
NG_013358.1:g.139575C>T
NG_013358.2:g.139575C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.*25C>T	ENSP00000468516.4:n.*25C>T
ENST00000651901.2:c.*25C>T	ENSP00000498922.2:n.*25C>T
ENST00000698359.1:c.*25C>T	ENSP00000513682.1:n.*25C>T
ENST00000698360.1:c.*25C>T	ENSP00000513683.1:n.*25C>T
ENST00000698361.1:c.*135C>T	ENSP00000513684.1:n.*135C>T
ENST00000698362.1:c.*644C>T	ENSP00000513685.1:n.*644C>T
ENST00000698426.1:c.*25C>T	ENSP00000513713.1:n.*25C>T
ENST00000698427.1:c.*25C>T	ENSP00000513714.1:n.*25C>T
ENST00000698428.1:c.*25C>T	ENSP00000513715.1:n.*25C>T
ENST00000698429.1:n.1390C>T
ENST00000698430.1:c.1757C>T
ENST00000698431.1:c.1244C>T	ENSP00000513717.1:n.1244C>T
ENST00000698432.1:c.1316C>T
ENST00000244137.12:c.*25C>T MANE Select	ENSP00000244137.5:n.*25C>T
ENST00000588328.6:c.1562C>T
ENST00000651901.1:c.1593C>T
ENST00000244137.11:c.*25C>T	ENSP00000244137.5:n.*25C>T
ENST00000397032.8:c.*25C>T	ENSP00000380226.3:n.*25C>T
ENST00000436370.7:c.*25C>T	ENSP00000391890.2:n.*25C>T
ENST00000589598.5:n.232C>T
ENST00000591968.1:n.579C>T
ENST00000593085.1:n.1394C>T
NM_000285.3:c.*25C>T	NP_000276.2:n.*25C>T
NM_001166056.1:c.*25C>T	NP_001159528.1:n.*25C>T
NM_001166057.1:c.*25C>T	NP_001159529.1:n.*25C>T
NM_000285.4:c.*25C>T MANE Select	NP_000276.2:n.*25C>T
NM_001166056.2:c.*25C>T	NP_001159528.1:n.*25C>T
NM_001166057.2:c.*25C>T	NP_001159529.1:n.*25C>T