Canonical Allele Identifier: CA1803280991

Gene: PDP1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.93923535T= , CM000670.2:g.93923535T=	GRCh38
NC_000008.10:g.94935763T= , CM000670.1:g.94935763T=	GRCh37
NC_000008.9:g.95004939T=	NCBI36
NG_012233.1:g.11602T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297598.5:c.1476T= MANE Select	ENSP00000297598.4:p.Phe492=
ENST00000297598.4:c.1476T=	ENSP00000297598.4:p.Phe492=
ENST00000396200.3:c.1551T=	ENSP00000379503.3:p.Phe517=
ENST00000517764.1:c.1476T=	ENSP00000430380.1:p.Phe492=
ENST00000520728.5:c.1476T=	ENSP00000428317.1:p.Phe492=
NM_001161779.1:c.1551T=	NP_001155251.1:p.Phe517=
NM_001161780.1:c.1551T=	NP_001155252.1:p.Phe517=
NM_001161781.1:c.1476T=	NP_001155253.1:p.Phe492=
NM_018444.3:c.1476T=	NP_060914.2:p.Phe492=
XM_011517135.1:c.1530T=	XP_011515437.1:p.Phe510=
XM_011517136.1:c.1476T=	XP_011515438.1:p.Phe492=
XM_011517137.1:c.1476T=	XP_011515439.1:p.Phe492=
XM_011517135.2:c.1530T=	XP_011515437.1:p.Phe510=
XM_011517136.2:c.1476T=	XP_011515438.1:p.Phe492=
XM_017013588.1:c.1638T=	XP_016869077.1:p.Phe546=
NM_018444.4:c.1476T= MANE Select	NP_060914.2:p.Phe492=
NM_001161780.2:c.1551T=	NP_001155252.1:p.Phe517=
NM_001161781.2:c.1476T=	NP_001155253.1:p.Phe492=
NM_001161779.2:c.1551T=	NP_001155251.1:p.Phe517=