Canonical Allele Identifier: CA506686725

Gene: PEPD

Linked Data

• MyVariant Identifiers: chr19:g.33878250C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33387344C>T , CM000681.2:g.33387344C>T	GRCh38
NC_000019.9:g.33878250C>T , CM000681.1:g.33878250C>T	GRCh37
NC_000019.8:g.38570090C>T	NCBI36
NG_013358.1:g.139550G>A
NG_013358.2:g.139550G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.1548G>A	ENSP00000468516.4:p.Ter516=
ENST00000651901.2:c.1572G>A	ENSP00000498922.2:p.Ter524=
ENST00000698359.1:c.1437G>A	ENSP00000513682.1:p.Ter479=
ENST00000698360.1:c.1533G>A	ENSP00000513683.1:p.Ter511=
ENST00000698361.1:c.*110G>A	ENSP00000513684.1:n.*110G>A
ENST00000698362.1:c.*619G>A	ENSP00000513685.1:n.*619G>A
ENST00000698426.1:c.1161G>A	ENSP00000513713.1:p.Ter387=
ENST00000698427.1:c.1524G>A	ENSP00000513714.1:p.Ter508=
ENST00000698428.1:c.1161G>A	ENSP00000513715.1:p.Ter387=
ENST00000698429.1:n.1365G>A
ENST00000698430.1:c.1732G>A
ENST00000698431.1:c.1219G>A	ENSP00000513717.1:n.1219G>A
ENST00000698432.1:c.1291G>A
ENST00000244137.12:c.1482G>A MANE Select	ENSP00000244137.5:p.Ter494=
ENST00000588328.6:c.1537G>A
ENST00000651901.1:c.1568G>A
ENST00000244137.11:c.1482G>A	ENSP00000244137.5:p.Ter494=
ENST00000397032.8:c.1359G>A	ENSP00000380226.3:p.Ter453=
ENST00000436370.7:c.1290G>A	ENSP00000391890.2:p.Ter430=
ENST00000589598.5:n.207G>A
ENST00000591968.1:n.554G>A
ENST00000593085.1:n.1369G>A
NM_000285.3:c.1482G>A	NP_000276.2:p.Ter494=
NM_001166056.1:c.1359G>A	NP_001159528.1:p.Ter453=
NM_001166057.1:c.1290G>A	NP_001159529.1:p.Ter430=
NM_000285.4:c.1482G>A MANE Select	NP_000276.2:p.Ter494=
NM_001166056.2:c.1359G>A	NP_001159528.1:p.Ter453=
NM_001166057.2:c.1290G>A	NP_001159529.1:p.Ter430=