Canonical Allele Identifier: CA645556619

Gene: PIK3R1

Linked Data

• dbSNP Id: rs2112276979
• COSMIC: COSM1578561 ; COSM1578562 ; COSM1578563

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.68295304_68295309del , CM000667.2:g.68295304_68295309del	GRCh38
NC_000005.9:g.67591132_67591137del , CM000667.1:g.67591132_67591137del	GRCh37
NC_000005.8:g.67626888_67626893del	NCBI36
NG_012849.2:g.84549_84554del

Transcript Alleles

HGVS	Amino-acid change
ENST00000320694.13:c.825_830del	ENSP00000323512.8:p.Thr276_Arg277del
ENST00000336483.10:c.915_920del	ENSP00000338554.5:p.Thr306_Arg307del
ENST00000517643.2:c.1725_1730del	ENSP00000513333.1:p.Thr576_Arg577del
ENST00000517698.6:c.*695_*700del	ENSP00000430424.1:n.*695_*700del
ENST00000521657.6:c.1725_1730del	ENSP00000429277.1:p.Thr576_Arg577del
ENST00000522084.6:c.915_920del	ENSP00000429766.2:p.Thr306_Arg307del
ENST00000697457.1:c.1650_1655del	ENSP00000513315.1:p.Thr551_Arg552del
ENST00000697458.1:c.1725_1730del	ENSP00000513316.1:p.Thr576_Arg577del
ENST00000697460.1:c.1200_1205del	ENSP00000513318.1:p.Thr401_Arg402del
ENST00000697461.1:c.1725_1730del	ENSP00000513319.1:p.Thr576_Arg577del
ENST00000697462.1:c.915_920del	ENSP00000513320.1:p.Thr306_Arg307del
ENST00000697463.1:n.1366_1371del
ENST00000697464.1:c.*691_*696del	ENSP00000513322.1:n.*691_*696del
ENST00000697465.1:c.762_767del	ENSP00000513323.1:p.Thr255_Arg256del
ENST00000697466.1:c.732_737del	ENSP00000513324.1:p.Thr245_Arg246del
ENST00000697467.1:c.636_641del	ENSP00000513325.1:p.Thr213_Arg214del
ENST00000697468.1:c.708_713del	ENSP00000513326.1:p.Thr237_Arg238del
ENST00000697469.1:c.417_422del	ENSP00000513327.1:p.Thr140_Arg141del
ENST00000697470.1:c.321_326del	ENSP00000513328.1:p.Thr108_Arg109del
ENST00000697557.1:c.708_713del	ENSP00000513335.1:p.Thr237_Arg238del
ENST00000521381.6:c.1725_1730del MANE Select	ENSP00000428056.1:p.Thr576_Arg577del
ENST00000320694.12:c.825_830del	ENSP00000323512.8:p.Thr276_Arg277del
ENST00000336483.9:c.915_920del	ENSP00000338554.5:p.Thr306_Arg307del
ENST00000517698.5:c.*695_*700del	ENSP00000430424.1:n.*695_*700del
ENST00000518813.5:n.2268_2273del
ENST00000520550.1:n.1124_1129del
ENST00000521381.5:c.1725_1730del	ENSP00000428056.1:p.Thr576_Arg577del
ENST00000521657.5:c.1725_1730del	ENSP00000429277.1:p.Thr576_Arg577del
ENST00000523872.1:c.636_641del	ENSP00000430098.1:p.Thr213_Arg214del
NM_001242466.1:c.636_641del	NP_001229395.1:p.Thr213_Arg214del
NM_181504.3:c.915_920del	NP_852556.2:p.Thr306_Arg307del
NM_181523.2:c.1725_1730del	NP_852664.1:p.Thr576_Arg577del
NM_181524.1:c.825_830del	NP_852665.1:p.Thr276_Arg277del
XM_005248542.2:c.1725_1730del	XP_005248599.1:p.Thr576_Arg577del
XM_011543493.1:c.1398_1403del	XP_011541795.1:p.Thr467_Arg468del
XM_005248542.3:c.1725_1730del	XP_005248599.1:p.Thr576_Arg577del
XM_011543493.3:c.1398_1403del	XP_011541795.1:p.Thr467_Arg468del
XM_017009585.2:c.1725_1730del	XP_016865074.1:p.Thr576_Arg577del
XM_017009586.1:c.1452_1457del	XP_016865075.1:p.Thr485_Arg486del
NM_181523.3:c.1725_1730del MANE Select	NP_852664.1:p.Thr576_Arg577del
NM_001242466.2:c.636_641del	NP_001229395.1:p.Thr213_Arg214del
NM_181504.4:c.915_920del	NP_852556.2:p.Thr306_Arg307del
NM_181524.2:c.825_830del	NP_852665.1:p.Thr276_Arg277del