Canonical Allele Identifier: CA405219707

Gene: PEPD

Linked Data

• MyVariant Identifiers: chr19:g.33878355G>C (hg19) ; chr19:g.33387449G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33387449G>C , CM000681.2:g.33387449G>C	GRCh38
NC_000019.9:g.33878355G>C , CM000681.1:g.33878355G>C	GRCh37
NC_000019.8:g.38570195G>C	NCBI36
NG_013358.1:g.139445C>G
NG_013358.2:g.139445C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.1443C>G	ENSP00000468516.4:p.Asp481Glu
ENST00000651901.2:c.1467C>G	ENSP00000498922.2:p.Asp489Glu
ENST00000698359.1:c.1332C>G	ENSP00000513682.1:p.Asp444Glu
ENST00000698360.1:c.1428C>G	ENSP00000513683.1:p.Asp476Glu
ENST00000698361.1:c.*5C>G	ENSP00000513684.1:n.*5C>G
ENST00000698362.1:c.*514C>G	ENSP00000513685.1:n.*514C>G
ENST00000698426.1:c.1056C>G	ENSP00000513713.1:p.Asp352Glu
ENST00000698427.1:c.1419C>G	ENSP00000513714.1:p.Asp473Glu
ENST00000698428.1:c.1056C>G	ENSP00000513715.1:p.Asp352Glu
ENST00000698429.1:n.1260C>G
ENST00000698430.1:c.1627C>G
ENST00000698431.1:c.1114C>G	ENSP00000513717.1:n.1114C>G
ENST00000698432.1:c.1186C>G
ENST00000698433.1:n.839C>G
ENST00000244137.12:c.1377C>G MANE Select	ENSP00000244137.5:p.Asp459Glu
ENST00000588328.6:c.1432C>G
ENST00000651901.1:c.1463C>G
ENST00000244137.11:c.1377C>G	ENSP00000244137.5:p.Asp459Glu
ENST00000397032.8:c.1254C>G	ENSP00000380226.3:p.Asp418Glu
ENST00000436370.7:c.1185C>G	ENSP00000391890.2:p.Asp395Glu
ENST00000589598.5:n.102C>G
ENST00000591968.1:n.449C>G
ENST00000593085.1:n.1264C>G
NM_000285.3:c.1377C>G	NP_000276.2:p.Asp459Glu
NM_001166056.1:c.1254C>G	NP_001159528.1:p.Asp418Glu
NM_001166057.1:c.1185C>G	NP_001159529.1:p.Asp395Glu
NM_000285.4:c.1377C>G MANE Select	NP_000276.2:p.Asp459Glu
NM_001166056.2:c.1254C>G	NP_001159528.1:p.Asp418Glu
NM_001166057.2:c.1185C>G	NP_001159529.1:p.Asp395Glu