Canonical Allele Identifier: CA2332735659

Gene: PEPD

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33464006G= , CM000681.2:g.33464006G=	GRCh38
NC_000019.9:g.33954912G= , CM000681.1:g.33954912G=	GRCh37
NC_000019.8:g.38646752G=	NCBI36
NG_013358.1:g.62888C=
NG_013358.2:g.62888C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000588328.7:c.605C=	ENSP00000468516.4:p.Ser202=
ENST00000651646.2:c.605C=	ENSP00000498950.2:p.Ser202=
ENST00000651901.2:c.605C=	ENSP00000498922.2:p.Ser202=
ENST00000698359.1:c.560C=	ENSP00000513682.1:p.Ser187=
ENST00000698360.1:c.605C=	ENSP00000513683.1:p.Ser202=
ENST00000698361.1:c.605C=	ENSP00000513684.1:p.Ser202=
ENST00000698362.1:c.605C=	ENSP00000513685.1:p.Ser202=
ENST00000698363.1:n.668C=
ENST00000698364.1:n.668C=
ENST00000698365.1:n.668C=
ENST00000698426.1:c.284C=	ENSP00000513713.1:p.Ser95=
ENST00000698427.1:c.647C=	ENSP00000513714.1:p.Ser216=
ENST00000698428.1:c.284C=	ENSP00000513715.1:p.Ser95=
ENST00000698430.1:c.855C=
ENST00000698431.1:c.342C=	ENSP00000513717.1:n.342C=
ENST00000698432.1:c.414C=
ENST00000698435.1:c.293C=	ENSP00000513719.1:p.Ser98=
ENST00000698436.1:c.*217C=	ENSP00000513720.1:n.*217C=
ENST00000698437.1:n.588C=
ENST00000698438.1:n.587C=
ENST00000698439.1:c.462C=	ENSP00000513721.1:n.462C=
ENST00000244137.12:c.605C= MANE Select	ENSP00000244137.5:p.Ser202=
ENST00000588328.6:c.594C=
ENST00000590731.6:n.280C=
ENST00000651646.1:c.603C=
ENST00000651901.1:c.601C=
ENST00000244137.11:c.605C=	ENSP00000244137.5:p.Ser202=
ENST00000397032.8:c.548+14040C=	ENSP00000380226.3:n.548+14040C=
ENST00000436370.7:c.413C=	ENSP00000391890.2:p.Ser138=
ENST00000588328.5:c.96C=
ENST00000588719.5:n.240C=
ENST00000590408.1:c.323C=
ENST00000590731.5:n.280C=
ENST00000590755.6:c.432C=	ENSP00000476667.1:n.432C=
ENST00000593163.5:n.770C=
ENST00000609145.5:c.38C=	ENSP00000476514.1:p.Ser13=
NM_000285.3:c.605C=	NP_000276.2:p.Ser202=
NM_001166056.1:c.548+14040C=	NP_001159528.1:n.548+14040C=
NM_001166057.1:c.413C=	NP_001159529.1:p.Ser138=
NM_000285.4:c.605C= MANE Select	NP_000276.2:p.Ser202=
NM_001166056.2:c.548+14040C=	NP_001159528.1:n.548+14040C=
NM_001166057.2:c.413C=	NP_001159529.1:p.Ser138=