Canonical Allele Identifier: CA2332706145

Gene: PEPD

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33401855C= , CM000681.2:g.33401855C=	GRCh38
NC_000019.9:g.33892761C= , CM000681.1:g.33892761C=	GRCh37
NC_000019.8:g.38584601C=	NCBI36
NG_013358.1:g.125039G=
NG_013358.2:g.125039G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000588328.7:c.833G=	ENSP00000468516.4:p.Gly278=
ENST00000651901.2:c.833G=	ENSP00000498922.2:p.Gly278=
ENST00000698359.1:c.788G=	ENSP00000513682.1:p.Gly263=
ENST00000698360.1:c.884G=	ENSP00000513683.1:p.Gly295=
ENST00000698361.1:c.833G=	ENSP00000513684.1:p.Gly278=
ENST00000698362.1:c.833G=	ENSP00000513685.1:p.Gly278=
ENST00000698363.1:n.896G=
ENST00000698364.1:n.896G=
ENST00000698365.1:n.896G=
ENST00000698426.1:c.512G=	ENSP00000513713.1:p.Gly171=
ENST00000698427.1:c.875G=	ENSP00000513714.1:p.Gly292=
ENST00000698428.1:c.512G=	ENSP00000513715.1:p.Gly171=
ENST00000698429.1:n.716G=
ENST00000698430.1:c.1083G=
ENST00000698431.1:c.570G=	ENSP00000513717.1:n.570G=
ENST00000698432.1:c.642G=
ENST00000698433.1:n.295G=
ENST00000698434.1:n.320G=
ENST00000698435.1:c.521G=	ENSP00000513719.1:p.Gly174=
ENST00000244137.12:c.833G= MANE Select	ENSP00000244137.5:p.Gly278=
ENST00000588328.6:c.822G=
ENST00000590731.6:n.508G=
ENST00000651901.1:c.829G=
ENST00000244137.11:c.833G=	ENSP00000244137.5:p.Gly278=
ENST00000397032.8:c.710G=	ENSP00000380226.3:p.Gly237=
ENST00000436370.7:c.641G=	ENSP00000391890.2:p.Gly214=
ENST00000588328.5:c.324G=
ENST00000588719.5:n.468G=
ENST00000590731.5:n.508G=
ENST00000593163.5:n.998G=
ENST00000609145.5:c.266G=	ENSP00000476514.1:p.Gly89=
NM_000285.3:c.833G=	NP_000276.2:p.Gly278=
NM_001166056.1:c.710G=	NP_001159528.1:p.Gly237=
NM_001166057.1:c.641G=	NP_001159529.1:p.Gly214=
NM_000285.4:c.833G= MANE Select	NP_000276.2:p.Gly278=
NM_001166056.2:c.710G=	NP_001159528.1:p.Gly237=
NM_001166057.2:c.641G=	NP_001159529.1:p.Gly214=