Canonical Allele Identifier: CA405224821

Gene: PEPD

Linked Data

• MyVariant Identifiers: chr19:g.33892774G>C (hg19) ; chr19:g.33401868G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33401868G>C , CM000681.2:g.33401868G>C	GRCh38
NC_000019.9:g.33892774G>C , CM000681.1:g.33892774G>C	GRCh37
NC_000019.8:g.38584614G>C	NCBI36
NG_013358.1:g.125026C>G
NG_013358.2:g.125026C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000588328.7:c.820C>G	ENSP00000468516.4:p.Leu274Val
ENST00000651901.2:c.820C>G	ENSP00000498922.2:p.Leu274Val
ENST00000698359.1:c.775C>G	ENSP00000513682.1:p.Leu259Val
ENST00000698360.1:c.871C>G	ENSP00000513683.1:p.Leu291Val
ENST00000698361.1:c.820C>G	ENSP00000513684.1:p.Leu274Val
ENST00000698362.1:c.820C>G	ENSP00000513685.1:p.Leu274Val
ENST00000698363.1:n.883C>G
ENST00000698364.1:n.883C>G
ENST00000698365.1:n.883C>G
ENST00000698426.1:c.499C>G	ENSP00000513713.1:p.Leu167Val
ENST00000698427.1:c.862C>G	ENSP00000513714.1:p.Leu288Val
ENST00000698428.1:c.499C>G	ENSP00000513715.1:p.Leu167Val
ENST00000698429.1:n.703C>G
ENST00000698430.1:c.1070C>G
ENST00000698431.1:c.557C>G	ENSP00000513717.1:n.557C>G
ENST00000698432.1:c.629C>G
ENST00000698433.1:n.282C>G
ENST00000698434.1:n.307C>G
ENST00000698435.1:c.508C>G	ENSP00000513719.1:p.Leu170Val
ENST00000244137.12:c.820C>G MANE Select	ENSP00000244137.5:p.Leu274Val
ENST00000588328.6:c.809C>G
ENST00000590731.6:n.495C>G
ENST00000651901.1:c.816C>G
ENST00000244137.11:c.820C>G	ENSP00000244137.5:p.Leu274Val
ENST00000397032.8:c.697C>G	ENSP00000380226.3:p.Leu233Val
ENST00000436370.7:c.628C>G	ENSP00000391890.2:p.Leu210Val
ENST00000588328.5:c.311C>G
ENST00000588719.5:n.455C>G
ENST00000590731.5:n.495C>G
ENST00000593163.5:n.985C>G
ENST00000609145.5:c.253C>G	ENSP00000476514.1:p.Leu85Val
NM_000285.3:c.820C>G	NP_000276.2:p.Leu274Val
NM_001166056.1:c.697C>G	NP_001159528.1:p.Leu233Val
NM_001166057.1:c.628C>G	NP_001159529.1:p.Leu210Val
NM_000285.4:c.820C>G MANE Select	NP_000276.2:p.Leu274Val
NM_001166056.2:c.697C>G	NP_001159528.1:p.Leu233Val
NM_001166057.2:c.628C>G	NP_001159529.1:p.Leu210Val