Canonical Allele Identifier: CA2332735663

Gene: PEPD

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33464016T= , CM000681.2:g.33464016T=	GRCh38
NC_000019.9:g.33954922T= , CM000681.1:g.33954922T=	GRCh37
NC_000019.8:g.38646762T=	NCBI36
NG_013358.1:g.62878A=
NG_013358.2:g.62878A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000588328.7:c.595A=	ENSP00000468516.4:p.Asn199=
ENST00000651646.2:c.595A=	ENSP00000498950.2:p.Asn199=
ENST00000651901.2:c.595A=	ENSP00000498922.2:p.Asn199=
ENST00000698359.1:c.550A=	ENSP00000513682.1:p.Asn184=
ENST00000698360.1:c.595A=	ENSP00000513683.1:p.Asn199=
ENST00000698361.1:c.595A=	ENSP00000513684.1:p.Asn199=
ENST00000698362.1:c.595A=	ENSP00000513685.1:p.Asn199=
ENST00000698363.1:n.658A=
ENST00000698364.1:n.658A=
ENST00000698365.1:n.658A=
ENST00000698426.1:c.274A=	ENSP00000513713.1:p.Asn92=
ENST00000698427.1:c.637A=	ENSP00000513714.1:p.Asn213=
ENST00000698428.1:c.274A=	ENSP00000513715.1:p.Asn92=
ENST00000698430.1:c.845A=
ENST00000698431.1:c.332A=	ENSP00000513717.1:n.332A=
ENST00000698432.1:c.404A=
ENST00000698435.1:c.283A=	ENSP00000513719.1:p.Asn95=
ENST00000698436.1:c.*207A=	ENSP00000513720.1:n.*207A=
ENST00000698437.1:n.578A=
ENST00000698438.1:n.577A=
ENST00000698439.1:c.452A=	ENSP00000513721.1:n.452A=
ENST00000244137.12:c.595A= MANE Select	ENSP00000244137.5:p.Asn199=
ENST00000588328.6:c.584A=
ENST00000590731.6:n.270A=
ENST00000651646.1:c.593A=
ENST00000651901.1:c.591A=
ENST00000244137.11:c.595A=	ENSP00000244137.5:p.Asn199=
ENST00000397032.8:c.548+14030A=	ENSP00000380226.3:n.548+14030A=
ENST00000436370.7:c.403A=	ENSP00000391890.2:p.Asn135=
ENST00000588328.5:c.86A=
ENST00000588719.5:n.230A=
ENST00000590408.1:c.313A=
ENST00000590731.5:n.270A=
ENST00000590755.6:c.422A=	ENSP00000476667.1:n.422A=
ENST00000593163.5:n.760A=
ENST00000609145.5:c.28A=	ENSP00000476514.1:p.Asn10=
NM_000285.3:c.595A=	NP_000276.2:p.Asn199=
NM_001166056.1:c.548+14030A=	NP_001159528.1:n.548+14030A=
NM_001166057.1:c.403A=	NP_001159529.1:p.Asn135=
NM_000285.4:c.595A= MANE Select	NP_000276.2:p.Asn199=
NM_001166056.2:c.548+14030A=	NP_001159528.1:n.548+14030A=
NM_001166057.2:c.403A=	NP_001159529.1:p.Asn135=