Canonical Allele Identifier: CA2841335683
Gene: PIK3R1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.68295337A>T , CM000667.2:g.68295337A>T GRCh38
NC_000005.9:g.67591165A>T , CM000667.1:g.67591165A>T GRCh37
NC_000005.8:g.67626921A>T NCBI36
NG_012849.2:g.84582A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000320694.13:c.845+13A>T ENSP00000323512.8:n.845+13A>T
ENST00000336483.10:c.935+13A>T ENSP00000338554.5:n.935+13A>T
ENST00000517643.2:c.1745+13A>T ENSP00000513333.1:n.1745+13A>T
ENST00000517698.6:c.*715+13A>T ENSP00000430424.1:n.*715+13A>T
ENST00000521657.6:c.1745+13A>T ENSP00000429277.1:n.1745+13A>T
ENST00000522084.6:c.935+13A>T ENSP00000429766.2:n.935+13A>T
ENST00000697457.1:c.1670+13A>T ENSP00000513315.1:n.1670+13A>T
ENST00000697458.1:c.1745+13A>T ENSP00000513316.1:n.1745+13A>T
ENST00000697460.1:c.1220+13A>T ENSP00000513318.1:n.1220+13A>T
ENST00000697461.1:c.1745+13A>T ENSP00000513319.1:n.1745+13A>T
ENST00000697462.1:c.935+13A>T ENSP00000513320.1:n.935+13A>T
ENST00000697463.1:n.1386+13A>T
ENST00000697464.1:c.*711+13A>T ENSP00000513322.1:n.*711+13A>T
ENST00000697465.1:c.782+13A>T ENSP00000513323.1:n.782+13A>T
ENST00000697466.1:c.752+13A>T ENSP00000513324.1:n.752+13A>T
ENST00000697467.1:c.656+13A>T ENSP00000513325.1:n.656+13A>T
ENST00000697468.1:c.728+13A>T ENSP00000513326.1:n.728+13A>T
ENST00000697469.1:c.437+13A>T ENSP00000513327.1:n.437+13A>T
ENST00000697470.1:c.341+13A>T ENSP00000513328.1:n.341+13A>T
ENST00000697557.1:c.728+13A>T ENSP00000513335.1:n.728+13A>T
ENST00000521381.6:c.1745+13A>T MANE Select ENSP00000428056.1:n.1745+13A>T
ENST00000320694.12:c.845+13A>T ENSP00000323512.8:n.845+13A>T
ENST00000336483.9:c.935+13A>T ENSP00000338554.5:n.935+13A>T
ENST00000517698.5:c.*715+13A>T ENSP00000430424.1:n.*715+13A>T
ENST00000518813.5:n.2288+13A>T
ENST00000520550.1:n.1144+13A>T
ENST00000521381.5:c.1745+13A>T ENSP00000428056.1:n.1745+13A>T
ENST00000521657.5:c.1745+13A>T ENSP00000429277.1:n.1745+13A>T
ENST00000523872.1:c.656+13A>T ENSP00000430098.1:n.656+13A>T
NM_001242466.1:c.656+13A>T NP_001229395.1:n.656+13A>T
NM_181504.3:c.935+13A>T NP_852556.2:n.935+13A>T
NM_181523.2:c.1745+13A>T NP_852664.1:n.1745+13A>T
NM_181524.1:c.845+13A>T NP_852665.1:n.845+13A>T
XM_005248542.2:c.1745+13A>T XP_005248599.1:n.1745+13A>T
XM_011543493.1:c.1418+13A>T XP_011541795.1:n.1418+13A>T
XM_005248542.3:c.1745+13A>T XP_005248599.1:n.1745+13A>T
XM_011543493.3:c.1418+13A>T XP_011541795.1:n.1418+13A>T
XM_017009585.2:c.1745+13A>T XP_016865074.1:n.1745+13A>T
XM_017009586.1:c.1472+13A>T XP_016865075.1:n.1472+13A>T
NM_181523.3:c.1745+13A>T MANE Select NP_852664.1:n.1745+13A>T
NM_001242466.2:c.656+13A>T NP_001229395.1:n.656+13A>T
NM_181504.4:c.935+13A>T NP_852556.2:n.935+13A>T
NM_181524.2:c.845+13A>T NP_852665.1:n.845+13A>T