Canonical Allele Identifier: CA1803280777

Gene: PDP1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.93922903G= , CM000670.2:g.93922903G=	GRCh38
NC_000008.10:g.94935131G= , CM000670.1:g.94935131G=	GRCh37
NC_000008.9:g.95004307G=	NCBI36
NG_012233.1:g.10970G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297598.5:c.844G= MANE Select	ENSP00000297598.4:p.Val282=
ENST00000297598.4:c.844G=	ENSP00000297598.4:p.Val282=
ENST00000396200.3:c.919G=	ENSP00000379503.3:p.Val307=
ENST00000517764.1:c.844G=	ENSP00000430380.1:p.Val282=
ENST00000520728.5:c.844G=	ENSP00000428317.1:p.Val282=
NM_001161779.1:c.919G=	NP_001155251.1:p.Val307=
NM_001161780.1:c.919G=	NP_001155252.1:p.Val307=
NM_001161781.1:c.844G=	NP_001155253.1:p.Val282=
NM_018444.3:c.844G=	NP_060914.2:p.Val282=
XM_011517135.1:c.898G=	XP_011515437.1:p.Val300=
XM_011517136.1:c.844G=	XP_011515438.1:p.Val282=
XM_011517137.1:c.844G=	XP_011515439.1:p.Val282=
XM_011517135.2:c.898G=	XP_011515437.1:p.Val300=
XM_011517136.2:c.844G=	XP_011515438.1:p.Val282=
XM_017013588.1:c.1006G=	XP_016869077.1:p.Val336=
NM_018444.4:c.844G= MANE Select	NP_060914.2:p.Val282=
NM_001161780.2:c.919G=	NP_001155252.1:p.Val307=
NM_001161781.2:c.844G=	NP_001155253.1:p.Val282=
NM_001161779.2:c.919G=	NP_001155251.1:p.Val307=