Canonical Allele Identifier: CA2332735661

Gene: PEPD

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000588328.7:c.597T=	ENSP00000468516.4:p.Asn199=
ENST00000651646.2:c.597T=	ENSP00000498950.2:p.Asn199=
ENST00000651901.2:c.597T=	ENSP00000498922.2:p.Asn199=
ENST00000698359.1:c.552T=	ENSP00000513682.1:p.Asn184=
ENST00000698360.1:c.597T=	ENSP00000513683.1:p.Asn199=
ENST00000698361.1:c.597T=	ENSP00000513684.1:p.Asn199=
ENST00000698362.1:c.597T=	ENSP00000513685.1:p.Asn199=
ENST00000698363.1:n.660T=
ENST00000698364.1:n.660T=
ENST00000698365.1:n.660T=
ENST00000698426.1:c.276T=	ENSP00000513713.1:p.Asn92=
ENST00000698427.1:c.639T=	ENSP00000513714.1:p.Asn213=
ENST00000698428.1:c.276T=	ENSP00000513715.1:p.Asn92=
ENST00000698430.1:c.847T=
ENST00000698431.1:c.334T=	ENSP00000513717.1:n.334T=
ENST00000698432.1:c.406T=
ENST00000698435.1:c.285T=	ENSP00000513719.1:p.Asn95=
ENST00000698436.1:c.*209T=	ENSP00000513720.1:n.*209T=
ENST00000698437.1:n.580T=
ENST00000698438.1:n.579T=
ENST00000698439.1:c.454T=	ENSP00000513721.1:n.454T=
ENST00000244137.12:c.597T= MANE Select	ENSP00000244137.5:p.Asn199=
ENST00000588328.6:c.586T=
ENST00000590731.6:n.272T=
ENST00000651646.1:c.595T=
ENST00000651901.1:c.593T=
ENST00000244137.11:c.597T=	ENSP00000244137.5:p.Asn199=
ENST00000397032.8:c.548+14032T=	ENSP00000380226.3:n.548+14032T=
ENST00000436370.7:c.405T=	ENSP00000391890.2:p.Asn135=
ENST00000588328.5:c.88T=
ENST00000588719.5:n.232T=
ENST00000590408.1:c.315T=
ENST00000590731.5:n.272T=
ENST00000590755.6:c.424T=	ENSP00000476667.1:n.424T=
ENST00000593163.5:n.762T=
ENST00000609145.5:c.30T=	ENSP00000476514.1:p.Asn10=
NM_000285.3:c.597T=	NP_000276.2:p.Asn199=
NM_001166056.1:c.548+14032T=	NP_001159528.1:n.548+14032T=
NM_001166057.1:c.405T=	NP_001159529.1:p.Asn135=
NM_000285.4:c.597T= MANE Select	NP_000276.2:p.Asn199=
NM_001166056.2:c.548+14032T=	NP_001159528.1:n.548+14032T=
NM_001166057.2:c.405T=	NP_001159529.1:p.Asn135=