Canonical Allele Identifier: CA2332706116

Gene: PEPD

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33401799T= , CM000681.2:g.33401799T=	GRCh38
NC_000019.9:g.33892705T= , CM000681.1:g.33892705T=	GRCh37
NC_000019.8:g.38584545T=	NCBI36
NG_013358.1:g.125095A=
NG_013358.2:g.125095A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.889A=	ENSP00000468516.4:p.Lys297=
ENST00000651901.2:c.889A=	ENSP00000498922.2:p.Lys297=
ENST00000698359.1:c.844A=	ENSP00000513682.1:p.Lys282=
ENST00000698360.1:c.940A=	ENSP00000513683.1:p.Lys314=
ENST00000698361.1:c.889A=	ENSP00000513684.1:p.Lys297=
ENST00000698362.1:c.889A=	ENSP00000513685.1:p.Lys297=
ENST00000698363.1:n.952A=
ENST00000698364.1:n.952A=
ENST00000698365.1:n.952A=
ENST00000698426.1:c.568A=	ENSP00000513713.1:p.Lys190=
ENST00000698427.1:c.931A=	ENSP00000513714.1:p.Lys311=
ENST00000698428.1:c.568A=	ENSP00000513715.1:p.Lys190=
ENST00000698429.1:n.772A=
ENST00000698430.1:c.1139A=
ENST00000698431.1:c.626A=	ENSP00000513717.1:n.626A=
ENST00000698432.1:c.698A=
ENST00000698433.1:n.351A=
ENST00000698434.1:n.376A=
ENST00000698435.1:c.577A=	ENSP00000513719.1:p.Lys193=
ENST00000244137.12:c.889A= MANE Select	ENSP00000244137.5:p.Lys297=
ENST00000588328.6:c.878A=
ENST00000590731.6:n.564A=
ENST00000651901.1:c.885A=
ENST00000244137.11:c.889A=	ENSP00000244137.5:p.Lys297=
ENST00000397032.8:c.766A=	ENSP00000380226.3:p.Lys256=
ENST00000436370.7:c.697A=	ENSP00000391890.2:p.Lys233=
ENST00000588328.5:c.380A=
NM_000285.3:c.889A=	NP_000276.2:p.Lys297=
NM_001166056.1:c.766A=	NP_001159528.1:p.Lys256=
NM_001166057.1:c.697A=	NP_001159529.1:p.Lys233=
NM_000285.4:c.889A= MANE Select	NP_000276.2:p.Lys297=
NM_001166056.2:c.766A=	NP_001159528.1:p.Lys256=
NM_001166057.2:c.697A=	NP_001159529.1:p.Lys233=