Canonical Allele Identifier: CA1553406140
Gene: PIK3R1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.68295184C= , CM000667.2:g.68295184C= GRCh38
NC_000005.9:g.67591012C= , CM000667.1:g.67591012C= GRCh37
NC_000005.8:g.67626768C= NCBI36
NG_012849.2:g.84429C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320694.13:c.705C= ENSP00000323512.8:p.Ile235=
ENST00000336483.10:c.795C= ENSP00000338554.5:p.Ile265=
ENST00000517643.2:c.1605C= ENSP00000513333.1:p.Ile535=
ENST00000517698.6:c.*575C= ENSP00000430424.1:n.*575C=
ENST00000521657.6:c.1605C= ENSP00000429277.1:p.Ile535=
ENST00000522084.6:c.795C= ENSP00000429766.2:p.Ile265=
ENST00000697457.1:c.1530C= ENSP00000513315.1:p.Ile510=
ENST00000697458.1:c.1605C= ENSP00000513316.1:p.Ile535=
ENST00000697460.1:c.1080C= ENSP00000513318.1:p.Ile360=
ENST00000697461.1:c.1605C= ENSP00000513319.1:p.Ile535=
ENST00000697462.1:c.795C= ENSP00000513320.1:p.Ile265=
ENST00000697463.1:n.1246C=
ENST00000697464.1:c.*571C= ENSP00000513322.1:n.*571C=
ENST00000697465.1:c.642C= ENSP00000513323.1:p.Ile214=
ENST00000697466.1:c.612C= ENSP00000513324.1:p.Ile204=
ENST00000697467.1:c.516C= ENSP00000513325.1:p.Ile172=
ENST00000697468.1:c.588C= ENSP00000513326.1:p.Ile196=
ENST00000697469.1:c.297C= ENSP00000513327.1:p.Ile99=
ENST00000697470.1:c.201C= ENSP00000513328.1:p.Ile67=
ENST00000697557.1:c.588C= ENSP00000513335.1:p.Ile196=
ENST00000521381.6:c.1605C= MANE Select ENSP00000428056.1:p.Ile535=
ENST00000320694.12:c.705C= ENSP00000323512.8:p.Ile235=
ENST00000336483.9:c.795C= ENSP00000338554.5:p.Ile265=
ENST00000517698.5:c.*575C= ENSP00000430424.1:n.*575C=
ENST00000518813.5:n.2148C=
ENST00000520550.1:n.1004C=
ENST00000521381.5:c.1605C= ENSP00000428056.1:p.Ile535=
ENST00000521657.5:c.1605C= ENSP00000429277.1:p.Ile535=
ENST00000523872.1:c.516C= ENSP00000430098.1:p.Ile172=
NM_001242466.1:c.516C= NP_001229395.1:p.Ile172=
NM_181504.3:c.795C= NP_852556.2:p.Ile265=
NM_181523.2:c.1605C= NP_852664.1:p.Ile535=
NM_181524.1:c.705C= NP_852665.1:p.Ile235=
XM_005248542.2:c.1605C= XP_005248599.1:p.Ile535=
XM_011543493.1:c.1278C= XP_011541795.1:p.Ile426=
XM_005248542.3:c.1605C= XP_005248599.1:p.Ile535=
XM_011543493.3:c.1278C= XP_011541795.1:p.Ile426=
XM_017009585.2:c.1605C= XP_016865074.1:p.Ile535=
XM_017009586.1:c.1332C= XP_016865075.1:p.Ile444=
NM_181523.3:c.1605C= MANE Select NP_852664.1:p.Ile535=
NM_001242466.2:c.516C= NP_001229395.1:p.Ile172=
NM_181504.4:c.795C= NP_852556.2:p.Ile265=
NM_181524.2:c.705C= NP_852665.1:p.Ile235=