Canonical Allele Identifier: CA444672818
Gene: PIK3R1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.68295303dup , CM000667.2:g.68295303dup GRCh38
NC_000005.9:g.67591131dup , CM000667.1:g.67591131dup GRCh37
NC_000005.8:g.67626887dup NCBI36
NG_012849.2:g.84548dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000320694.13:c.824dup ENSP00000323512.8:p.Thr276AspfsTer26
ENST00000336483.10:c.914dup ENSP00000338554.5:p.Thr306AspfsTer26
ENST00000517643.2:c.1724dup ENSP00000513333.1:p.Thr576AspfsTer26
ENST00000517698.6:c.*694dup ENSP00000430424.1:n.*694dup
ENST00000521657.6:c.1724dup ENSP00000429277.1:p.Thr576AspfsTer26
ENST00000522084.6:c.914dup ENSP00000429766.2:p.Thr306AspfsTer26
ENST00000697457.1:c.1649dup ENSP00000513315.1:p.Thr551AspfsTer26
ENST00000697458.1:c.1724dup ENSP00000513316.1:p.Thr576AspfsTer26
ENST00000697460.1:c.1199dup ENSP00000513318.1:p.Thr401AspfsTer26
ENST00000697461.1:c.1724dup ENSP00000513319.1:p.Thr576AspfsTer26
ENST00000697462.1:c.914dup ENSP00000513320.1:p.Thr306AspfsTer26
ENST00000697463.1:n.1365dup
ENST00000697464.1:c.*690dup ENSP00000513322.1:n.*690dup
ENST00000697465.1:c.761dup ENSP00000513323.1:p.Thr255AspfsTer26
ENST00000697466.1:c.731dup ENSP00000513324.1:p.Thr245AspfsTer26
ENST00000697467.1:c.635dup ENSP00000513325.1:p.Thr213AspfsTer26
ENST00000697468.1:c.707dup ENSP00000513326.1:p.Thr237AspfsTer26
ENST00000697469.1:c.416dup ENSP00000513327.1:p.Thr140AspfsTer26
ENST00000697470.1:c.320dup ENSP00000513328.1:p.Thr108AspfsTer26
ENST00000697557.1:c.707dup ENSP00000513335.1:p.Thr237AspfsTer26
ENST00000521381.6:c.1724dup MANE Select ENSP00000428056.1:p.Thr576AspfsTer26
ENST00000320694.12:c.824dup ENSP00000323512.8:p.Thr276AspfsTer26
ENST00000336483.9:c.914dup ENSP00000338554.5:p.Thr306AspfsTer26
ENST00000517698.5:c.*694dup ENSP00000430424.1:n.*694dup
ENST00000518813.5:n.2267dup
ENST00000520550.1:n.1123dup
ENST00000521381.5:c.1724dup ENSP00000428056.1:p.Thr576AspfsTer26
ENST00000521657.5:c.1724dup ENSP00000429277.1:p.Thr576AspfsTer26
ENST00000523872.1:c.635dup ENSP00000430098.1:p.Thr213AspfsTer26
NM_001242466.1:c.635dup NP_001229395.1:p.Thr213AspfsTer26
NM_181504.3:c.914dup NP_852556.2:p.Thr306AspfsTer26
NM_181523.2:c.1724dup NP_852664.1:p.Thr576AspfsTer26
NM_181524.1:c.824dup NP_852665.1:p.Thr276AspfsTer26
XM_005248542.2:c.1724dup XP_005248599.1:p.Thr576AspfsTer26
XM_011543493.1:c.1397dup XP_011541795.1:p.Thr467AspfsTer26
XM_005248542.3:c.1724dup XP_005248599.1:p.Thr576AspfsTer26
XM_011543493.3:c.1397dup XP_011541795.1:p.Thr467AspfsTer26
XM_017009585.2:c.1724dup XP_016865074.1:p.Thr576AspfsTer26
XM_017009586.1:c.1451dup XP_016865075.1:p.Thr485AspfsTer26
NM_181523.3:c.1724dup MANE Select NP_852664.1:p.Thr576AspfsTer26
NM_001242466.2:c.635dup NP_001229395.1:p.Thr213AspfsTer26
NM_181504.4:c.914dup NP_852556.2:p.Thr306AspfsTer26
NM_181524.2:c.824dup NP_852665.1:p.Thr276AspfsTer26