Canonical Allele Identifier: CA405219786

Gene: PEPD

Linked Data

• MyVariant Identifiers: chr19:g.33878386A>T (hg19) ; chr19:g.33387480A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33387480A>T , CM000681.2:g.33387480A>T	GRCh38
NC_000019.9:g.33878386A>T , CM000681.1:g.33878386A>T	GRCh37
NC_000019.8:g.38570226A>T	NCBI36
NG_013358.1:g.139414T>A
NG_013358.2:g.139414T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.1412T>A	ENSP00000468516.4:p.Val471Asp
ENST00000651901.2:c.1436T>A	ENSP00000498922.2:p.Val479Asp
ENST00000698359.1:c.1301T>A	ENSP00000513682.1:p.Val434Asp
ENST00000698360.1:c.1397T>A	ENSP00000513683.1:p.Val466Asp
ENST00000698361.1:c.1462T>A	ENSP00000513684.1:p.Ser488Thr
ENST00000698362.1:c.*483T>A	ENSP00000513685.1:n.*483T>A
ENST00000698426.1:c.1025T>A	ENSP00000513713.1:p.Val342Asp
ENST00000698427.1:c.1388T>A	ENSP00000513714.1:p.Val463Asp
ENST00000698428.1:c.1025T>A	ENSP00000513715.1:p.Val342Asp
ENST00000698429.1:n.1229T>A
ENST00000698430.1:c.1596T>A
ENST00000698431.1:c.1083T>A	ENSP00000513717.1:n.1083T>A
ENST00000698432.1:c.1155T>A
ENST00000698433.1:n.808T>A
ENST00000244137.12:c.1346T>A MANE Select	ENSP00000244137.5:p.Val449Asp
ENST00000588328.6:c.1401T>A
ENST00000651901.1:c.1432T>A
ENST00000244137.11:c.1346T>A	ENSP00000244137.5:p.Val449Asp
ENST00000397032.8:c.1223T>A	ENSP00000380226.3:p.Val408Asp
ENST00000436370.7:c.1154T>A	ENSP00000391890.2:p.Val385Asp
ENST00000589598.5:n.71T>A
ENST00000591968.1:n.418T>A
ENST00000593085.1:n.1233T>A
NM_000285.3:c.1346T>A	NP_000276.2:p.Val449Asp
NM_001166056.1:c.1223T>A	NP_001159528.1:p.Val408Asp
NM_001166057.1:c.1154T>A	NP_001159529.1:p.Val385Asp
NM_000285.4:c.1346T>A MANE Select	NP_000276.2:p.Val449Asp
NM_001166056.2:c.1223T>A	NP_001159528.1:p.Val408Asp
NM_001166057.2:c.1154T>A	NP_001159529.1:p.Val385Asp