Canonical Allele Identifier: CA506687832

Gene: PEPD

Linked Data

• MyVariant Identifiers: chr19:g.33892663G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33401757G>T , CM000681.2:g.33401757G>T	GRCh38
NC_000019.9:g.33892663G>T , CM000681.1:g.33892663G>T	GRCh37
NC_000019.8:g.38584503G>T	NCBI36
NG_013358.1:g.125137C>A
NG_013358.2:g.125137C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000588328.7:c.931C>A	ENSP00000468516.4:p.Arg311=
ENST00000651901.2:c.931C>A	ENSP00000498922.2:p.Arg311=
ENST00000698359.1:c.886C>A	ENSP00000513682.1:p.Arg296=
ENST00000698360.1:c.982C>A	ENSP00000513683.1:p.Arg328=
ENST00000698361.1:c.931C>A	ENSP00000513684.1:p.Arg311=
ENST00000698362.1:c.931C>A	ENSP00000513685.1:p.Arg311=
ENST00000698363.1:n.994C>A
ENST00000698364.1:n.994C>A
ENST00000698365.1:n.994C>A
ENST00000698426.1:c.610C>A	ENSP00000513713.1:p.Arg204=
ENST00000698427.1:c.973C>A	ENSP00000513714.1:p.Arg325=
ENST00000698428.1:c.610C>A	ENSP00000513715.1:p.Arg204=
ENST00000698429.1:n.814C>A
ENST00000698430.1:c.1181C>A
ENST00000698431.1:c.668C>A	ENSP00000513717.1:n.668C>A
ENST00000698432.1:c.740C>A
ENST00000698433.1:n.393C>A
ENST00000698434.1:n.418C>A
ENST00000244137.12:c.931C>A MANE Select	ENSP00000244137.5:p.Arg311=
ENST00000588328.6:c.920C>A
ENST00000590731.6:n.606C>A
ENST00000651901.1:c.927C>A
ENST00000244137.11:c.931C>A	ENSP00000244137.5:p.Arg311=
ENST00000397032.8:c.808C>A	ENSP00000380226.3:p.Arg270=
ENST00000436370.7:c.739C>A	ENSP00000391890.2:p.Arg247=
ENST00000588328.5:c.422C>A
NM_000285.3:c.931C>A	NP_000276.2:p.Arg311=
NM_001166056.1:c.808C>A	NP_001159528.1:p.Arg270=
NM_001166057.1:c.739C>A	NP_001159529.1:p.Arg247=
NM_000285.4:c.931C>A MANE Select	NP_000276.2:p.Arg311=
NM_001166056.2:c.808C>A	NP_001159528.1:p.Arg270=
NM_001166057.2:c.739C>A	NP_001159529.1:p.Arg247=