Canonical Allele Identifier: CA405224791

Gene: PEPD

Linked Data

• MyVariant Identifiers: chr19:g.33892767T>C (hg19) ; chr19:g.33401861T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33401861T>C , CM000681.2:g.33401861T>C	GRCh38
NC_000019.9:g.33892767T>C , CM000681.1:g.33892767T>C	GRCh37
NC_000019.8:g.38584607T>C	NCBI36
NG_013358.1:g.125033A>G
NG_013358.2:g.125033A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000588328.7:c.827A>G	ENSP00000468516.4:p.Asp276Gly
ENST00000651901.2:c.827A>G	ENSP00000498922.2:p.Asp276Gly
ENST00000698359.1:c.782A>G	ENSP00000513682.1:p.Asp261Gly
ENST00000698360.1:c.878A>G	ENSP00000513683.1:p.Asp293Gly
ENST00000698361.1:c.827A>G	ENSP00000513684.1:p.Asp276Gly
ENST00000698362.1:c.827A>G	ENSP00000513685.1:p.Asp276Gly
ENST00000698363.1:n.890A>G
ENST00000698364.1:n.890A>G
ENST00000698365.1:n.890A>G
ENST00000698426.1:c.506A>G	ENSP00000513713.1:p.Asp169Gly
ENST00000698427.1:c.869A>G	ENSP00000513714.1:p.Asp290Gly
ENST00000698428.1:c.506A>G	ENSP00000513715.1:p.Asp169Gly
ENST00000698429.1:n.710A>G
ENST00000698430.1:c.1077A>G
ENST00000698431.1:c.564A>G	ENSP00000513717.1:n.564A>G
ENST00000698432.1:c.636A>G
ENST00000698433.1:n.289A>G
ENST00000698434.1:n.314A>G
ENST00000698435.1:c.515A>G	ENSP00000513719.1:p.Asp172Gly
ENST00000244137.12:c.827A>G MANE Select	ENSP00000244137.5:p.Asp276Gly
ENST00000588328.6:c.816A>G
ENST00000590731.6:n.502A>G
ENST00000651901.1:c.823A>G
ENST00000244137.11:c.827A>G	ENSP00000244137.5:p.Asp276Gly
ENST00000397032.8:c.704A>G	ENSP00000380226.3:p.Asp235Gly
ENST00000436370.7:c.635A>G	ENSP00000391890.2:p.Asp212Gly
ENST00000588328.5:c.318A>G
ENST00000588719.5:n.462A>G
ENST00000590731.5:n.502A>G
ENST00000593163.5:n.992A>G
ENST00000609145.5:c.260A>G	ENSP00000476514.1:p.Asp87Gly
NM_000285.3:c.827A>G	NP_000276.2:p.Asp276Gly
NM_001166056.1:c.704A>G	NP_001159528.1:p.Asp235Gly
NM_001166057.1:c.635A>G	NP_001159529.1:p.Asp212Gly
NM_000285.4:c.827A>G MANE Select	NP_000276.2:p.Asp276Gly
NM_001166056.2:c.704A>G	NP_001159528.1:p.Asp235Gly
NM_001166057.2:c.635A>G	NP_001159529.1:p.Asp212Gly