Canonical Allele Identifier: CA1553406180
Gene: PIK3R1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.68295311_68295317delinsGACCAAT , CM000667.2:g.68295311_68295317delinsGACCAAT GRCh38
NC_000005.9:g.67591139_67591145delinsGACCAAT , CM000667.1:g.67591139_67591145delinsGACCAAT GRCh37
NC_000005.8:g.67626895_67626901delinsGACCAAT NCBI36
NG_012849.2:g.84556_84562delinsGACCAAT

Transcript Alleles

HGVS Amino-acid change
ENST00000320694.13:c.832_838delinsGACCAAT ENSP00000323512.8:p.Asp278=
ENST00000336483.10:c.922_928delinsGACCAAT ENSP00000338554.5:p.Asp308=
ENST00000517643.2:c.1732_1738delinsGACCAAT ENSP00000513333.1:p.Asp578=
ENST00000517698.6:c.*702_*708delinsGACCAAT ENSP00000430424.1:n.*702_*708delinsGACCAA...
ENST00000521657.6:c.1732_1738delinsGACCAAT ENSP00000429277.1:p.Asp578=
ENST00000522084.6:c.922_928delinsGACCAAT ENSP00000429766.2:p.Asp308=
ENST00000697457.1:c.1657_1663delinsGACCAAT ENSP00000513315.1:p.Asp553=
ENST00000697458.1:c.1732_1738delinsGACCAAT ENSP00000513316.1:p.Asp578=
ENST00000697460.1:c.1207_1213delinsGACCAAT ENSP00000513318.1:p.Asp403=
ENST00000697461.1:c.1732_1738delinsGACCAAT ENSP00000513319.1:p.Asp578=
ENST00000697462.1:c.922_928delinsGACCAAT ENSP00000513320.1:p.Asp308=
ENST00000697463.1:n.1373_1379delinsGACCAAT
ENST00000697464.1:c.*698_*704delinsGACCAAT ENSP00000513322.1:n.*698_*704delinsGACCAA...
ENST00000697465.1:c.769_775delinsGACCAAT ENSP00000513323.1:p.Asp257=
ENST00000697466.1:c.739_745delinsGACCAAT ENSP00000513324.1:p.Asp247=
ENST00000697467.1:c.643_649delinsGACCAAT ENSP00000513325.1:p.Asp215=
ENST00000697468.1:c.715_721delinsGACCAAT ENSP00000513326.1:p.Asp239=
ENST00000697469.1:c.424_430delinsGACCAAT ENSP00000513327.1:p.Asp142=
ENST00000697470.1:c.328_334delinsGACCAAT ENSP00000513328.1:p.Asp110=
ENST00000697557.1:c.715_721delinsGACCAAT ENSP00000513335.1:p.Asp239=
ENST00000521381.6:c.1732_1738delinsGACCAAT MANE Select ENSP00000428056.1:p.Asp578=
ENST00000320694.12:c.832_838delinsGACCAAT ENSP00000323512.8:p.Asp278=
ENST00000336483.9:c.922_928delinsGACCAAT ENSP00000338554.5:p.Asp308=
ENST00000517698.5:c.*702_*708delinsGACCAAT ENSP00000430424.1:n.*702_*708delinsGACCAA...
ENST00000518813.5:n.2275_2281delinsGACCAAT
ENST00000520550.1:n.1131_1137delinsGACCAAT
ENST00000521381.5:c.1732_1738delinsGACCAAT ENSP00000428056.1:p.Asp578=
ENST00000521657.5:c.1732_1738delinsGACCAAT ENSP00000429277.1:p.Asp578=
ENST00000523872.1:c.643_649delinsGACCAAT ENSP00000430098.1:p.Asp215=
NM_001242466.1:c.643_649delinsGACCAAT NP_001229395.1:p.Asp215=
NM_181504.3:c.922_928delinsGACCAAT NP_852556.2:p.Asp308=
NM_181523.2:c.1732_1738delinsGACCAAT NP_852664.1:p.Asp578=
NM_181524.1:c.832_838delinsGACCAAT NP_852665.1:p.Asp278=
XM_005248542.2:c.1732_1738delinsGACCAAT XP_005248599.1:p.Asp578=
XM_011543493.1:c.1405_1411delinsGACCAAT XP_011541795.1:p.Asp469=
XM_005248542.3:c.1732_1738delinsGACCAAT XP_005248599.1:p.Asp578=
XM_011543493.3:c.1405_1411delinsGACCAAT XP_011541795.1:p.Asp469=
XM_017009585.2:c.1732_1738delinsGACCAAT XP_016865074.1:p.Asp578=
XM_017009586.1:c.1459_1465delinsGACCAAT XP_016865075.1:p.Asp487=
NM_181523.3:c.1732_1738delinsGACCAAT MANE Select NP_852664.1:p.Asp578=
NM_001242466.2:c.643_649delinsGACCAAT NP_001229395.1:p.Asp215=
NM_181504.4:c.922_928delinsGACCAAT NP_852556.2:p.Asp308=
NM_181524.2:c.832_838delinsGACCAAT NP_852665.1:p.Asp278=