Canonical Allele Identifier: CA405230737

Gene: PEPD

Linked Data

• MyVariant Identifiers: chr19:g.33954920A>C (hg19) ; chr19:g.33464014A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33464014A>C , CM000681.2:g.33464014A>C	GRCh38
NC_000019.9:g.33954920A>C , CM000681.1:g.33954920A>C	GRCh37
NC_000019.8:g.38646760A>C	NCBI36
NG_013358.1:g.62880T>G
NG_013358.2:g.62880T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000588328.7:c.597T>G	ENSP00000468516.4:p.Asn199Lys
ENST00000651646.2:c.597T>G	ENSP00000498950.2:p.Asn199Lys
ENST00000651901.2:c.597T>G	ENSP00000498922.2:p.Asn199Lys
ENST00000698359.1:c.552T>G	ENSP00000513682.1:p.Asn184Lys
ENST00000698360.1:c.597T>G	ENSP00000513683.1:p.Asn199Lys
ENST00000698361.1:c.597T>G	ENSP00000513684.1:p.Asn199Lys
ENST00000698362.1:c.597T>G	ENSP00000513685.1:p.Asn199Lys
ENST00000698363.1:n.660T>G
ENST00000698364.1:n.660T>G
ENST00000698365.1:n.660T>G
ENST00000698426.1:c.276T>G	ENSP00000513713.1:p.Asn92Lys
ENST00000698427.1:c.639T>G	ENSP00000513714.1:p.Asn213Lys
ENST00000698428.1:c.276T>G	ENSP00000513715.1:p.Asn92Lys
ENST00000698430.1:c.847T>G
ENST00000698431.1:c.334T>G	ENSP00000513717.1:n.334T>G
ENST00000698432.1:c.406T>G
ENST00000698435.1:c.285T>G	ENSP00000513719.1:p.Asn95Lys
ENST00000698436.1:c.*209T>G	ENSP00000513720.1:n.*209T>G
ENST00000698437.1:n.580T>G
ENST00000698438.1:n.579T>G
ENST00000698439.1:c.454T>G	ENSP00000513721.1:n.454T>G
ENST00000244137.12:c.597T>G MANE Select	ENSP00000244137.5:p.Asn199Lys
ENST00000588328.6:c.586T>G
ENST00000590731.6:n.272T>G
ENST00000651646.1:c.595T>G
ENST00000651901.1:c.593T>G
ENST00000244137.11:c.597T>G	ENSP00000244137.5:p.Asn199Lys
ENST00000397032.8:c.548+14032T>G	ENSP00000380226.3:n.548+14032T>G
ENST00000436370.7:c.405T>G	ENSP00000391890.2:p.Asn135Lys
ENST00000588328.5:c.88T>G
ENST00000588719.5:n.232T>G
ENST00000590408.1:c.315T>G
ENST00000590731.5:n.272T>G
ENST00000590755.6:c.424T>G	ENSP00000476667.1:n.424T>G
ENST00000593163.5:n.762T>G
ENST00000609145.5:c.30T>G	ENSP00000476514.1:p.Asn10Lys
NM_000285.3:c.597T>G	NP_000276.2:p.Asn199Lys
NM_001166056.1:c.548+14032T>G	NP_001159528.1:n.548+14032T>G
NM_001166057.1:c.405T>G	NP_001159529.1:p.Asn135Lys
NM_000285.4:c.597T>G MANE Select	NP_000276.2:p.Asn199Lys
NM_001166056.2:c.548+14032T>G	NP_001159528.1:n.548+14032T>G
NM_001166057.2:c.405T>G	NP_001159529.1:p.Asn135Lys