Canonical Allele Identifier: CA506686739

Gene: PEPD

Linked Data

• MyVariant Identifiers: chr19:g.33878268G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33387362G>C , CM000681.2:g.33387362G>C	GRCh38
NC_000019.9:g.33878268G>C , CM000681.1:g.33878268G>C	GRCh37
NC_000019.8:g.38570108G>C	NCBI36
NG_013358.1:g.139532C>G
NG_013358.2:g.139532C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.1530C>G	ENSP00000468516.4:p.Pro510=
ENST00000651901.2:c.1554C>G	ENSP00000498922.2:p.Pro518=
ENST00000698359.1:c.1419C>G	ENSP00000513682.1:p.Pro473=
ENST00000698360.1:c.1515C>G	ENSP00000513683.1:p.Pro505=
ENST00000698361.1:c.*92C>G	ENSP00000513684.1:n.*92C>G
ENST00000698362.1:c.*601C>G	ENSP00000513685.1:n.*601C>G
ENST00000698426.1:c.1143C>G	ENSP00000513713.1:p.Pro381=
ENST00000698427.1:c.1506C>G	ENSP00000513714.1:p.Pro502=
ENST00000698428.1:c.1143C>G	ENSP00000513715.1:p.Pro381=
ENST00000698429.1:n.1347C>G
ENST00000698430.1:c.1714C>G
ENST00000698431.1:c.1201C>G	ENSP00000513717.1:n.1201C>G
ENST00000698432.1:c.1273C>G
ENST00000698433.1:n.926C>G
ENST00000244137.12:c.1464C>G MANE Select	ENSP00000244137.5:p.Pro488=
ENST00000588328.6:c.1519C>G
ENST00000651901.1:c.1550C>G
ENST00000244137.11:c.1464C>G	ENSP00000244137.5:p.Pro488=
ENST00000397032.8:c.1341C>G	ENSP00000380226.3:p.Pro447=
ENST00000436370.7:c.1272C>G	ENSP00000391890.2:p.Pro424=
ENST00000589598.5:n.189C>G
ENST00000591968.1:n.536C>G
ENST00000593085.1:n.1351C>G
NM_000285.3:c.1464C>G	NP_000276.2:p.Pro488=
NM_001166056.1:c.1341C>G	NP_001159528.1:p.Pro447=
NM_001166057.1:c.1272C>G	NP_001159529.1:p.Pro424=
NM_000285.4:c.1464C>G MANE Select	NP_000276.2:p.Pro488=
NM_001166056.2:c.1341C>G	NP_001159528.1:p.Pro447=
NM_001166057.2:c.1272C>G	NP_001159529.1:p.Pro424=