Canonical Allele Identifier: CA2332706097

Gene: PEPD

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33401756C= , CM000681.2:g.33401756C=	GRCh38
NC_000019.9:g.33892662C= , CM000681.1:g.33892662C=	GRCh37
NC_000019.8:g.38584502C=	NCBI36
NG_013358.1:g.125138G=
NG_013358.2:g.125138G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000588328.7:c.932G=	ENSP00000468516.4:p.Arg311=
ENST00000651901.2:c.932G=	ENSP00000498922.2:p.Arg311=
ENST00000698359.1:c.887G=	ENSP00000513682.1:p.Arg296=
ENST00000698360.1:c.983G=	ENSP00000513683.1:p.Arg328=
ENST00000698361.1:c.932G=	ENSP00000513684.1:p.Arg311=
ENST00000698362.1:c.932G=	ENSP00000513685.1:p.Arg311=
ENST00000698363.1:n.995G=
ENST00000698364.1:n.995G=
ENST00000698365.1:n.995G=
ENST00000698426.1:c.611G=	ENSP00000513713.1:p.Arg204=
ENST00000698427.1:c.974G=	ENSP00000513714.1:p.Arg325=
ENST00000698428.1:c.611G=	ENSP00000513715.1:p.Arg204=
ENST00000698429.1:n.815G=
ENST00000698430.1:c.1182G=
ENST00000698431.1:c.669G=	ENSP00000513717.1:n.669G=
ENST00000698432.1:c.741G=
ENST00000698433.1:n.394G=
ENST00000698434.1:n.419G=
ENST00000244137.12:c.932G= MANE Select	ENSP00000244137.5:p.Arg311=
ENST00000588328.6:c.921G=
ENST00000590731.6:n.607G=
ENST00000651901.1:c.928G=
ENST00000244137.11:c.932G=	ENSP00000244137.5:p.Arg311=
ENST00000397032.8:c.809G=	ENSP00000380226.3:p.Arg270=
ENST00000436370.7:c.740G=	ENSP00000391890.2:p.Arg247=
ENST00000588328.5:c.423G=
NM_000285.3:c.932G=	NP_000276.2:p.Arg311=
NM_001166056.1:c.809G=	NP_001159528.1:p.Arg270=
NM_001166057.1:c.740G=	NP_001159529.1:p.Arg247=
NM_000285.4:c.932G= MANE Select	NP_000276.2:p.Arg311=
NM_001166056.2:c.809G=	NP_001159528.1:p.Arg270=
NM_001166057.2:c.740G=	NP_001159529.1:p.Arg247=