Canonical Allele Identifier: CA1803281029

Gene: PDP1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.93923644G= , CM000670.2:g.93923644G=	GRCh38
NC_000008.10:g.94935872G= , CM000670.1:g.94935872G=	GRCh37
NC_000008.9:g.95005048G=	NCBI36
NG_012233.1:g.11711G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297598.5:c.1585G= MANE Select	ENSP00000297598.4:p.Val529=
ENST00000297598.4:c.1585G=	ENSP00000297598.4:p.Val529=
ENST00000396200.3:c.1660G=	ENSP00000379503.3:p.Val554=
ENST00000517764.1:c.1585G=	ENSP00000430380.1:p.Val529=
ENST00000520728.5:c.1585G=	ENSP00000428317.1:p.Val529=
NM_001161779.1:c.1660G=	NP_001155251.1:p.Val554=
NM_001161780.1:c.1660G=	NP_001155252.1:p.Val554=
NM_001161781.1:c.1585G=	NP_001155253.1:p.Val529=
NM_018444.3:c.1585G=	NP_060914.2:p.Val529=
XM_011517135.1:c.1639G=	XP_011515437.1:p.Val547=
XM_011517136.1:c.1585G=	XP_011515438.1:p.Val529=
XM_011517137.1:c.1585G=	XP_011515439.1:p.Val529=
XM_011517135.2:c.1639G=	XP_011515437.1:p.Val547=
XM_011517136.2:c.1585G=	XP_011515438.1:p.Val529=
XM_017013588.1:c.1747G=	XP_016869077.1:p.Val583=
NM_018444.4:c.1585G= MANE Select	NP_060914.2:p.Val529=
NM_001161780.2:c.1660G=	NP_001155252.1:p.Val554=
NM_001161781.2:c.1585G=	NP_001155253.1:p.Val529=
NM_001161779.2:c.1660G=	NP_001155251.1:p.Val554=