Canonical Allele Identifier: CA645553496

Gene: PDP1

Linked Data

• COSMIC: COSM2157375 ; COSM2157376

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.93923388_93923390del , CM000670.2:g.93923388_93923390del	GRCh38
NC_000008.10:g.94935616_94935618del , CM000670.1:g.94935616_94935618del	GRCh37
NC_000008.9:g.95004792_95004794del	NCBI36
NG_012233.1:g.11455_11457del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297598.5:c.1329_1331del MANE Select	ENSP00000297598.4:p.Gln444del
ENST00000297598.4:c.1329_1331del	ENSP00000297598.4:p.Gln444del
ENST00000396200.3:c.1404_1406del	ENSP00000379503.3:p.Gln469del
ENST00000517764.1:c.1329_1331del	ENSP00000430380.1:p.Gln444del
ENST00000520728.5:c.1329_1331del	ENSP00000428317.1:p.Gln444del
NM_001161779.1:c.1404_1406del	NP_001155251.1:p.Gln469del
NM_001161780.1:c.1404_1406del	NP_001155252.1:p.Gln469del
NM_001161781.1:c.1329_1331del	NP_001155253.1:p.Gln444del
NM_018444.3:c.1329_1331del	NP_060914.2:p.Gln444del
XM_011517135.1:c.1383_1385del	XP_011515437.1:p.Gln462del
XM_011517136.1:c.1329_1331del	XP_011515438.1:p.Gln444del
XM_011517137.1:c.1329_1331del	XP_011515439.1:p.Gln444del
XM_011517135.2:c.1383_1385del	XP_011515437.1:p.Gln462del
XM_011517136.2:c.1329_1331del	XP_011515438.1:p.Gln444del
XM_017013588.1:c.1491_1493del	XP_016869077.1:p.Gln498del
NM_018444.4:c.1329_1331del MANE Select	NP_060914.2:p.Gln444del
NM_001161780.2:c.1404_1406del	NP_001155252.1:p.Gln469del
NM_001161781.2:c.1329_1331del	NP_001155253.1:p.Gln444del
NM_001161779.2:c.1404_1406del	NP_001155251.1:p.Gln469del