Canonical Allele Identifier: CA645556602

Gene: PIK3R1

Linked Data

• COSMIC: COSM85885 ; COSM1069614 ; COSM1595473 ; COSM1595474

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.68295288_68295314del , CM000667.2:g.68295288_68295314del	GRCh38
NC_000005.9:g.67591116_67591142del , CM000667.1:g.67591116_67591142del	GRCh37
NC_000005.8:g.67626872_67626898del	NCBI36
NG_012849.2:g.84533_84559del

Transcript Alleles

HGVS	Amino-acid change
ENST00000320694.13:c.809_835del	ENSP00000323512.8:p.Leu270_Asp278del
ENST00000336483.10:c.899_925del	ENSP00000338554.5:p.Leu300_Asp308del
ENST00000517643.2:c.1709_1735del	ENSP00000513333.1:p.Leu570_Asp578del
ENST00000517698.6:c.*679_*705del	ENSP00000430424.1:n.*679_*705del
ENST00000521657.6:c.1709_1735del	ENSP00000429277.1:p.Leu570_Asp578del
ENST00000522084.6:c.899_925del	ENSP00000429766.2:p.Leu300_Asp308del
ENST00000697457.1:c.1634_1660del	ENSP00000513315.1:p.Leu545_Asp553del
ENST00000697458.1:c.1709_1735del	ENSP00000513316.1:p.Leu570_Asp578del
ENST00000697460.1:c.1184_1210del	ENSP00000513318.1:p.Leu395_Asp403del
ENST00000697461.1:c.1709_1735del	ENSP00000513319.1:p.Leu570_Asp578del
ENST00000697462.1:c.899_925del	ENSP00000513320.1:p.Leu300_Asp308del
ENST00000697463.1:n.1350_1376del
ENST00000697464.1:c.*675_*701del	ENSP00000513322.1:n.*675_*701del
ENST00000697465.1:c.746_772del	ENSP00000513323.1:p.Leu249_Asp257del
ENST00000697466.1:c.716_742del	ENSP00000513324.1:p.Leu239_Asp247del
ENST00000697467.1:c.620_646del	ENSP00000513325.1:p.Leu207_Asp215del
ENST00000697468.1:c.692_718del	ENSP00000513326.1:p.Leu231_Asp239del
ENST00000697469.1:c.401_427del	ENSP00000513327.1:p.Leu134_Asp142del
ENST00000697470.1:c.305_331del	ENSP00000513328.1:p.Leu102_Asp110del
ENST00000697557.1:c.692_718del	ENSP00000513335.1:p.Leu231_Asp239del
ENST00000521381.6:c.1709_1735del MANE Select	ENSP00000428056.1:p.Leu570_Asp578del
ENST00000320694.12:c.809_835del	ENSP00000323512.8:p.Leu270_Asp278del
ENST00000336483.9:c.899_925del	ENSP00000338554.5:p.Leu300_Asp308del
ENST00000517698.5:c.*679_*705del	ENSP00000430424.1:n.*679_*705del
ENST00000518813.5:n.2252_2278del
ENST00000520550.1:n.1108_1134del
ENST00000521381.5:c.1709_1735del	ENSP00000428056.1:p.Leu570_Asp578del
ENST00000521657.5:c.1709_1735del	ENSP00000429277.1:p.Leu570_Asp578del
ENST00000523872.1:c.620_646del	ENSP00000430098.1:p.Leu207_Asp215del
NM_001242466.1:c.620_646del	NP_001229395.1:p.Leu207_Asp215del
NM_181504.3:c.899_925del	NP_852556.2:p.Leu300_Asp308del
NM_181523.2:c.1709_1735del	NP_852664.1:p.Leu570_Asp578del
NM_181524.1:c.809_835del	NP_852665.1:p.Leu270_Asp278del
XM_005248542.2:c.1709_1735del	XP_005248599.1:p.Leu570_Asp578del
XM_011543493.1:c.1382_1408del	XP_011541795.1:p.Leu461_Asp469del
XM_005248542.3:c.1709_1735del	XP_005248599.1:p.Leu570_Asp578del
XM_011543493.3:c.1382_1408del	XP_011541795.1:p.Leu461_Asp469del
XM_017009585.2:c.1709_1735del	XP_016865074.1:p.Leu570_Asp578del
XM_017009586.1:c.1436_1462del	XP_016865075.1:p.Leu479_Asp487del
NM_181523.3:c.1709_1735del MANE Select	NP_852664.1:p.Leu570_Asp578del
NM_001242466.2:c.620_646del	NP_001229395.1:p.Leu207_Asp215del
NM_181504.4:c.899_925del	NP_852556.2:p.Leu300_Asp308del
NM_181524.2:c.809_835del	NP_852665.1:p.Leu270_Asp278del