Canonical Allele Identifier: CA1803280774

Gene: PDP1

Linked Data

• dbSNP Id: rs1810326385

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.93922901_93922906del , CM000670.2:g.93922901_93922906del	GRCh38
NC_000008.10:g.94935129_94935134del , CM000670.1:g.94935129_94935134del	GRCh37
NC_000008.9:g.95004305_95004310del	NCBI36
NG_012233.1:g.10968_10973del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297598.5:c.842_847del MANE Select	ENSP00000297598.4:p.Gly281_Val282del
ENST00000297598.4:c.842_847del	ENSP00000297598.4:p.Gly281_Val282del
ENST00000396200.3:c.917_922del	ENSP00000379503.3:p.Gly306_Val307del
ENST00000517764.1:c.842_847del	ENSP00000430380.1:p.Gly281_Val282del
ENST00000520728.5:c.842_847del	ENSP00000428317.1:p.Gly281_Val282del
NM_001161779.1:c.917_922del	NP_001155251.1:p.Gly306_Val307del
NM_001161780.1:c.917_922del	NP_001155252.1:p.Gly306_Val307del
NM_001161781.1:c.842_847del	NP_001155253.1:p.Gly281_Val282del
NM_018444.3:c.842_847del	NP_060914.2:p.Gly281_Val282del
XM_011517135.1:c.896_901del	XP_011515437.1:p.Gly299_Val300del
XM_011517136.1:c.842_847del	XP_011515438.1:p.Gly281_Val282del
XM_011517137.1:c.842_847del	XP_011515439.1:p.Gly281_Val282del
XM_011517135.2:c.896_901del	XP_011515437.1:p.Gly299_Val300del
XM_011517136.2:c.842_847del	XP_011515438.1:p.Gly281_Val282del
XM_017013588.1:c.1004_1009del	XP_016869077.1:p.Gly335_Val336del
NM_018444.4:c.842_847del MANE Select	NP_060914.2:p.Gly281_Val282del
NM_001161780.2:c.917_922del	NP_001155252.1:p.Gly306_Val307del
NM_001161781.2:c.842_847del	NP_001155253.1:p.Gly281_Val282del
NM_001161779.2:c.917_922del	NP_001155251.1:p.Gly306_Val307del