Canonical Allele Identifier: CA1803280949

Gene: PDP1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.93923432T= , CM000670.2:g.93923432T=	GRCh38
NC_000008.10:g.94935660T= , CM000670.1:g.94935660T=	GRCh37
NC_000008.9:g.95004836T=	NCBI36
NG_012233.1:g.11499T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297598.5:c.1373T= MANE Select	ENSP00000297598.4:p.Met458=
ENST00000297598.4:c.1373T=	ENSP00000297598.4:p.Met458=
ENST00000396200.3:c.1448T=	ENSP00000379503.3:p.Met483=
ENST00000517764.1:c.1373T=	ENSP00000430380.1:p.Met458=
ENST00000520728.5:c.1373T=	ENSP00000428317.1:p.Met458=
NM_001161779.1:c.1448T=	NP_001155251.1:p.Met483=
NM_001161780.1:c.1448T=	NP_001155252.1:p.Met483=
NM_001161781.1:c.1373T=	NP_001155253.1:p.Met458=
NM_018444.3:c.1373T=	NP_060914.2:p.Met458=
XM_011517135.1:c.1427T=	XP_011515437.1:p.Met476=
XM_011517136.1:c.1373T=	XP_011515438.1:p.Met458=
XM_011517137.1:c.1373T=	XP_011515439.1:p.Met458=
XM_011517135.2:c.1427T=	XP_011515437.1:p.Met476=
XM_011517136.2:c.1373T=	XP_011515438.1:p.Met458=
XM_017013588.1:c.1535T=	XP_016869077.1:p.Met512=
NM_018444.4:c.1373T= MANE Select	NP_060914.2:p.Met458=
NM_001161780.2:c.1448T=	NP_001155252.1:p.Met483=
NM_001161781.2:c.1373T=	NP_001155253.1:p.Met458=
NM_001161779.2:c.1448T=	NP_001155251.1:p.Met483=