Canonical Allele Identifier: CA1803280791

Gene: PDP1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.93922937G= , CM000670.2:g.93922937G=	GRCh38
NC_000008.10:g.94935165G= , CM000670.1:g.94935165G=	GRCh37
NC_000008.9:g.95004341G=	NCBI36
NG_012233.1:g.11004G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297598.5:c.878G= MANE Select	ENSP00000297598.4:p.Arg293=
ENST00000297598.4:c.878G=	ENSP00000297598.4:p.Arg293=
ENST00000396200.3:c.953G=	ENSP00000379503.3:p.Arg318=
ENST00000517764.1:c.878G=	ENSP00000430380.1:p.Arg293=
ENST00000520728.5:c.878G=	ENSP00000428317.1:p.Arg293=
NM_001161779.1:c.953G=	NP_001155251.1:p.Arg318=
NM_001161780.1:c.953G=	NP_001155252.1:p.Arg318=
NM_001161781.1:c.878G=	NP_001155253.1:p.Arg293=
NM_018444.3:c.878G=	NP_060914.2:p.Arg293=
XM_011517135.1:c.932G=	XP_011515437.1:p.Arg311=
XM_011517136.1:c.878G=	XP_011515438.1:p.Arg293=
XM_011517137.1:c.878G=	XP_011515439.1:p.Arg293=
XM_011517135.2:c.932G=	XP_011515437.1:p.Arg311=
XM_011517136.2:c.878G=	XP_011515438.1:p.Arg293=
XM_017013588.1:c.1040G=	XP_016869077.1:p.Arg347=
NM_018444.4:c.878G= MANE Select	NP_060914.2:p.Arg293=
NM_001161780.2:c.953G=	NP_001155252.1:p.Arg318=
NM_001161781.2:c.878G=	NP_001155253.1:p.Arg293=
NM_001161779.2:c.953G=	NP_001155251.1:p.Arg318=