Canonical Allele Identifier: CA645556623

Gene: PIK3R1

Linked Data

• COSMIC: COSM1069629 ; COSM1595612 ; COSM1595613

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.68295308_68295313del , CM000667.2:g.68295308_68295313del	GRCh38
NC_000005.9:g.67591136_67591141del , CM000667.1:g.67591136_67591141del	GRCh37
NC_000005.8:g.67626892_67626897del	NCBI36
NG_012849.2:g.84553_84558del

Transcript Alleles

HGVS	Amino-acid change
ENST00000320694.13:c.829_834del	ENSP00000323512.8:p.Arg277_Asp278del
ENST00000336483.10:c.919_924del	ENSP00000338554.5:p.Arg307_Asp308del
ENST00000517643.2:c.1729_1734del	ENSP00000513333.1:p.Arg577_Asp578del
ENST00000517698.6:c.*699_*704del	ENSP00000430424.1:n.*699_*704del
ENST00000521657.6:c.1729_1734del	ENSP00000429277.1:p.Arg577_Asp578del
ENST00000522084.6:c.919_924del	ENSP00000429766.2:p.Arg307_Asp308del
ENST00000697457.1:c.1654_1659del	ENSP00000513315.1:p.Arg552_Asp553del
ENST00000697458.1:c.1729_1734del	ENSP00000513316.1:p.Arg577_Asp578del
ENST00000697460.1:c.1204_1209del	ENSP00000513318.1:p.Arg402_Asp403del
ENST00000697461.1:c.1729_1734del	ENSP00000513319.1:p.Arg577_Asp578del
ENST00000697462.1:c.919_924del	ENSP00000513320.1:p.Arg307_Asp308del
ENST00000697463.1:n.1370_1375del
ENST00000697464.1:c.*695_*700del	ENSP00000513322.1:n.*695_*700del
ENST00000697465.1:c.766_771del	ENSP00000513323.1:p.Arg256_Asp257del
ENST00000697466.1:c.736_741del	ENSP00000513324.1:p.Arg246_Asp247del
ENST00000697467.1:c.640_645del	ENSP00000513325.1:p.Arg214_Asp215del
ENST00000697468.1:c.712_717del	ENSP00000513326.1:p.Arg238_Asp239del
ENST00000697469.1:c.421_426del	ENSP00000513327.1:p.Arg141_Asp142del
ENST00000697470.1:c.325_330del	ENSP00000513328.1:p.Arg109_Asp110del
ENST00000697557.1:c.712_717del	ENSP00000513335.1:p.Arg238_Asp239del
ENST00000521381.6:c.1729_1734del MANE Select	ENSP00000428056.1:p.Arg577_Asp578del
ENST00000320694.12:c.829_834del	ENSP00000323512.8:p.Arg277_Asp278del
ENST00000336483.9:c.919_924del	ENSP00000338554.5:p.Arg307_Asp308del
ENST00000517698.5:c.*699_*704del	ENSP00000430424.1:n.*699_*704del
ENST00000518813.5:n.2272_2277del
ENST00000520550.1:n.1128_1133del
ENST00000521381.5:c.1729_1734del	ENSP00000428056.1:p.Arg577_Asp578del
ENST00000521657.5:c.1729_1734del	ENSP00000429277.1:p.Arg577_Asp578del
ENST00000523872.1:c.640_645del	ENSP00000430098.1:p.Arg214_Asp215del
NM_001242466.1:c.640_645del	NP_001229395.1:p.Arg214_Asp215del
NM_181504.3:c.919_924del	NP_852556.2:p.Arg307_Asp308del
NM_181523.2:c.1729_1734del	NP_852664.1:p.Arg577_Asp578del
NM_181524.1:c.829_834del	NP_852665.1:p.Arg277_Asp278del
XM_005248542.2:c.1729_1734del	XP_005248599.1:p.Arg577_Asp578del
XM_011543493.1:c.1402_1407del	XP_011541795.1:p.Arg468_Asp469del
XM_005248542.3:c.1729_1734del	XP_005248599.1:p.Arg577_Asp578del
XM_011543493.3:c.1402_1407del	XP_011541795.1:p.Arg468_Asp469del
XM_017009585.2:c.1729_1734del	XP_016865074.1:p.Arg577_Asp578del
XM_017009586.1:c.1456_1461del	XP_016865075.1:p.Arg486_Asp487del
NM_181523.3:c.1729_1734del MANE Select	NP_852664.1:p.Arg577_Asp578del
NM_001242466.2:c.640_645del	NP_001229395.1:p.Arg214_Asp215del
NM_181504.4:c.919_924del	NP_852556.2:p.Arg307_Asp308del
NM_181524.2:c.829_834del	NP_852665.1:p.Arg277_Asp278del