Canonical Allele Identifier: CA645556600

Gene: PIK3R1

Linked Data

• COSMIC: COSM1717416

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.68295280_68295306del , CM000667.2:g.68295280_68295306del	GRCh38
NC_000005.9:g.67591108_67591134del , CM000667.1:g.67591108_67591134del	GRCh37
NC_000005.8:g.67626864_67626890del	NCBI36
NG_012849.2:g.84525_84551del

Transcript Alleles

HGVS	Amino-acid change
ENST00000320694.13:c.801_827del	ENSP00000323512.8:p.Pro268_Thr276del
ENST00000336483.10:c.891_917del	ENSP00000338554.5:p.Pro298_Thr306del
ENST00000517643.2:c.1701_1727del	ENSP00000513333.1:p.Pro568_Thr576del
ENST00000517698.6:c.*671_*697del	ENSP00000430424.1:n.*671_*697del
ENST00000521657.6:c.1701_1727del	ENSP00000429277.1:p.Pro568_Thr576del
ENST00000522084.6:c.891_917del	ENSP00000429766.2:p.Pro298_Thr306del
ENST00000697457.1:c.1626_1652del	ENSP00000513315.1:p.Pro543_Thr551del
ENST00000697458.1:c.1701_1727del	ENSP00000513316.1:p.Pro568_Thr576del
ENST00000697460.1:c.1176_1202del	ENSP00000513318.1:p.Pro393_Thr401del
ENST00000697461.1:c.1701_1727del	ENSP00000513319.1:p.Pro568_Thr576del
ENST00000697462.1:c.891_917del	ENSP00000513320.1:p.Pro298_Thr306del
ENST00000697463.1:n.1342_1368del
ENST00000697464.1:c.*667_*693del	ENSP00000513322.1:n.*667_*693del
ENST00000697465.1:c.738_764del	ENSP00000513323.1:p.Pro247_Thr255del
ENST00000697466.1:c.708_734del	ENSP00000513324.1:p.Pro237_Thr245del
ENST00000697467.1:c.612_638del	ENSP00000513325.1:p.Pro205_Thr213del
ENST00000697468.1:c.684_710del	ENSP00000513326.1:p.Pro229_Thr237del
ENST00000697469.1:c.393_419del	ENSP00000513327.1:p.Pro132_Thr140del
ENST00000697470.1:c.297_323del	ENSP00000513328.1:p.Pro100_Thr108del
ENST00000697557.1:c.684_710del	ENSP00000513335.1:p.Pro229_Thr237del
ENST00000521381.6:c.1701_1727del MANE Select	ENSP00000428056.1:p.Pro568_Thr576del
ENST00000320694.12:c.801_827del	ENSP00000323512.8:p.Pro268_Thr276del
ENST00000336483.9:c.891_917del	ENSP00000338554.5:p.Pro298_Thr306del
ENST00000517698.5:c.*671_*697del	ENSP00000430424.1:n.*671_*697del
ENST00000518813.5:n.2244_2270del
ENST00000520550.1:n.1100_1126del
ENST00000521381.5:c.1701_1727del	ENSP00000428056.1:p.Pro568_Thr576del
ENST00000521657.5:c.1701_1727del	ENSP00000429277.1:p.Pro568_Thr576del
ENST00000523872.1:c.612_638del	ENSP00000430098.1:p.Pro205_Thr213del
NM_001242466.1:c.612_638del	NP_001229395.1:p.Pro205_Thr213del
NM_181504.3:c.891_917del	NP_852556.2:p.Pro298_Thr306del
NM_181523.2:c.1701_1727del	NP_852664.1:p.Pro568_Thr576del
NM_181524.1:c.801_827del	NP_852665.1:p.Pro268_Thr276del
XM_005248542.2:c.1701_1727del	XP_005248599.1:p.Pro568_Thr576del
XM_011543493.1:c.1374_1400del	XP_011541795.1:p.Pro459_Thr467del
XM_005248542.3:c.1701_1727del	XP_005248599.1:p.Pro568_Thr576del
XM_011543493.3:c.1374_1400del	XP_011541795.1:p.Pro459_Thr467del
XM_017009585.2:c.1701_1727del	XP_016865074.1:p.Pro568_Thr576del
XM_017009586.1:c.1428_1454del	XP_016865075.1:p.Pro477_Thr485del
NM_181523.3:c.1701_1727del MANE Select	NP_852664.1:p.Pro568_Thr576del
NM_001242466.2:c.612_638del	NP_001229395.1:p.Pro205_Thr213del
NM_181504.4:c.891_917del	NP_852556.2:p.Pro298_Thr306del
NM_181524.2:c.801_827del	NP_852665.1:p.Pro268_Thr276del