Canonical Allele Identifier: CA405219421

Gene: PEPD

Linked Data

• MyVariant Identifiers: chr19:g.33878284T>A (hg19) ; chr19:g.33387378T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33387378T>A , CM000681.2:g.33387378T>A	GRCh38
NC_000019.9:g.33878284T>A , CM000681.1:g.33878284T>A	GRCh37
NC_000019.8:g.38570124T>A	NCBI36
NG_013358.1:g.139516A>T
NG_013358.2:g.139516A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.1514A>T	ENSP00000468516.4:p.Asp505Val
ENST00000651901.2:c.1538A>T	ENSP00000498922.2:p.Asp513Val
ENST00000698359.1:c.1403A>T	ENSP00000513682.1:p.Asp468Val
ENST00000698360.1:c.1499A>T	ENSP00000513683.1:p.Asp500Val
ENST00000698361.1:c.*76A>T	ENSP00000513684.1:n.*76A>T
ENST00000698362.1:c.*585A>T	ENSP00000513685.1:n.*585A>T
ENST00000698426.1:c.1127A>T	ENSP00000513713.1:p.Asp376Val
ENST00000698427.1:c.1490A>T	ENSP00000513714.1:p.Asp497Val
ENST00000698428.1:c.1127A>T	ENSP00000513715.1:p.Asp376Val
ENST00000698429.1:n.1331A>T
ENST00000698430.1:c.1698A>T
ENST00000698431.1:c.1185A>T	ENSP00000513717.1:n.1185A>T
ENST00000698432.1:c.1257A>T
ENST00000698433.1:n.910A>T
ENST00000244137.12:c.1448A>T MANE Select	ENSP00000244137.5:p.Asp483Val
ENST00000588328.6:c.1503A>T
ENST00000651901.1:c.1534A>T
ENST00000244137.11:c.1448A>T	ENSP00000244137.5:p.Asp483Val
ENST00000397032.8:c.1325A>T	ENSP00000380226.3:p.Asp442Val
ENST00000436370.7:c.1256A>T	ENSP00000391890.2:p.Asp419Val
ENST00000589598.5:n.173A>T
ENST00000591968.1:n.520A>T
ENST00000593085.1:n.1335A>T
NM_000285.3:c.1448A>T	NP_000276.2:p.Asp483Val
NM_001166056.1:c.1325A>T	NP_001159528.1:p.Asp442Val
NM_001166057.1:c.1256A>T	NP_001159529.1:p.Asp419Val
NM_000285.4:c.1448A>T MANE Select	NP_000276.2:p.Asp483Val
NM_001166056.2:c.1325A>T	NP_001159528.1:p.Asp442Val
NM_001166057.2:c.1256A>T	NP_001159529.1:p.Asp419Val