Canonical Allele Identifier: CA506686831

Gene: PEPD

Linked Data

• MyVariant Identifiers: chr19:g.33878385G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33387479G>T , CM000681.2:g.33387479G>T	GRCh38
NC_000019.9:g.33878385G>T , CM000681.1:g.33878385G>T	GRCh37
NC_000019.8:g.38570225G>T	NCBI36
NG_013358.1:g.139415C>A
NG_013358.2:g.139415C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.1413C>A	ENSP00000468516.4:p.Val471=
ENST00000651901.2:c.1437C>A	ENSP00000498922.2:p.Val479=
ENST00000698359.1:c.1302C>A	ENSP00000513682.1:p.Val434=
ENST00000698360.1:c.1398C>A	ENSP00000513683.1:p.Val466=
ENST00000698361.1:c.1463C>A	ENSP00000513684.1:p.Ser488Tyr
ENST00000698362.1:c.*484C>A	ENSP00000513685.1:n.*484C>A
ENST00000698426.1:c.1026C>A	ENSP00000513713.1:p.Val342=
ENST00000698427.1:c.1389C>A	ENSP00000513714.1:p.Val463=
ENST00000698428.1:c.1026C>A	ENSP00000513715.1:p.Val342=
ENST00000698429.1:n.1230C>A
ENST00000698430.1:c.1597C>A
ENST00000698431.1:c.1084C>A	ENSP00000513717.1:n.1084C>A
ENST00000698432.1:c.1156C>A
ENST00000698433.1:n.809C>A
ENST00000244137.12:c.1347C>A MANE Select	ENSP00000244137.5:p.Val449=
ENST00000588328.6:c.1402C>A
ENST00000651901.1:c.1433C>A
ENST00000244137.11:c.1347C>A	ENSP00000244137.5:p.Val449=
ENST00000397032.8:c.1224C>A	ENSP00000380226.3:p.Val408=
ENST00000436370.7:c.1155C>A	ENSP00000391890.2:p.Val385=
ENST00000589598.5:n.72C>A
ENST00000591968.1:n.419C>A
ENST00000593085.1:n.1234C>A
NM_000285.3:c.1347C>A	NP_000276.2:p.Val449=
NM_001166056.1:c.1224C>A	NP_001159528.1:p.Val408=
NM_001166057.1:c.1155C>A	NP_001159529.1:p.Val385=
NM_000285.4:c.1347C>A MANE Select	NP_000276.2:p.Val449=
NM_001166056.2:c.1224C>A	NP_001159528.1:p.Val408=
NM_001166057.2:c.1155C>A	NP_001159529.1:p.Val385=