Canonical Allele Identifier: CA405224764

Gene: PEPD

Linked Data

• MyVariant Identifiers: chr19:g.33892761C>A (hg19) ; chr19:g.33401855C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33401855C>A , CM000681.2:g.33401855C>A	GRCh38
NC_000019.9:g.33892761C>A , CM000681.1:g.33892761C>A	GRCh37
NC_000019.8:g.38584601C>A	NCBI36
NG_013358.1:g.125039G>T
NG_013358.2:g.125039G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000588328.7:c.833G>T	ENSP00000468516.4:p.Gly278Val
ENST00000651901.2:c.833G>T	ENSP00000498922.2:p.Gly278Val
ENST00000698359.1:c.788G>T	ENSP00000513682.1:p.Gly263Val
ENST00000698360.1:c.884G>T	ENSP00000513683.1:p.Gly295Val
ENST00000698361.1:c.833G>T	ENSP00000513684.1:p.Gly278Val
ENST00000698362.1:c.833G>T	ENSP00000513685.1:p.Gly278Val
ENST00000698363.1:n.896G>T
ENST00000698364.1:n.896G>T
ENST00000698365.1:n.896G>T
ENST00000698426.1:c.512G>T	ENSP00000513713.1:p.Gly171Val
ENST00000698427.1:c.875G>T	ENSP00000513714.1:p.Gly292Val
ENST00000698428.1:c.512G>T	ENSP00000513715.1:p.Gly171Val
ENST00000698429.1:n.716G>T
ENST00000698430.1:c.1083G>T
ENST00000698431.1:c.570G>T	ENSP00000513717.1:n.570G>T
ENST00000698432.1:c.642G>T
ENST00000698433.1:n.295G>T
ENST00000698434.1:n.320G>T
ENST00000698435.1:c.521G>T	ENSP00000513719.1:p.Gly174Val
ENST00000244137.12:c.833G>T MANE Select	ENSP00000244137.5:p.Gly278Val
ENST00000588328.6:c.822G>T
ENST00000590731.6:n.508G>T
ENST00000651901.1:c.829G>T
ENST00000244137.11:c.833G>T	ENSP00000244137.5:p.Gly278Val
ENST00000397032.8:c.710G>T	ENSP00000380226.3:p.Gly237Val
ENST00000436370.7:c.641G>T	ENSP00000391890.2:p.Gly214Val
ENST00000588328.5:c.324G>T
ENST00000588719.5:n.468G>T
ENST00000590731.5:n.508G>T
ENST00000593163.5:n.998G>T
ENST00000609145.5:c.266G>T	ENSP00000476514.1:p.Gly89Val
NM_000285.3:c.833G>T	NP_000276.2:p.Gly278Val
NM_001166056.1:c.710G>T	NP_001159528.1:p.Gly237Val
NM_001166057.1:c.641G>T	NP_001159529.1:p.Gly214Val
NM_000285.4:c.833G>T MANE Select	NP_000276.2:p.Gly278Val
NM_001166056.2:c.710G>T	NP_001159528.1:p.Gly237Val
NM_001166057.2:c.641G>T	NP_001159529.1:p.Gly214Val