Canonical Allele Identifier: CA1553406170
Gene: PIK3R1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.68295274C= , CM000667.2:g.68295274C= GRCh38
NC_000005.9:g.67591102C= , CM000667.1:g.67591102C= GRCh37
NC_000005.8:g.67626858C= NCBI36
NG_012849.2:g.84519C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320694.13:c.795C= ENSP00000323512.8:p.Ser265=
ENST00000336483.10:c.885C= ENSP00000338554.5:p.Ser295=
ENST00000517643.2:c.1695C= ENSP00000513333.1:p.Ser565=
ENST00000517698.6:c.*665C= ENSP00000430424.1:n.*665C=
ENST00000521657.6:c.1695C= ENSP00000429277.1:p.Ser565=
ENST00000522084.6:c.885C= ENSP00000429766.2:p.Ser295=
ENST00000697457.1:c.1620C= ENSP00000513315.1:p.Ser540=
ENST00000697458.1:c.1695C= ENSP00000513316.1:p.Ser565=
ENST00000697460.1:c.1170C= ENSP00000513318.1:p.Ser390=
ENST00000697461.1:c.1695C= ENSP00000513319.1:p.Ser565=
ENST00000697462.1:c.885C= ENSP00000513320.1:p.Ser295=
ENST00000697463.1:n.1336C=
ENST00000697464.1:c.*661C= ENSP00000513322.1:n.*661C=
ENST00000697465.1:c.732C= ENSP00000513323.1:p.Ser244=
ENST00000697466.1:c.702C= ENSP00000513324.1:p.Ser234=
ENST00000697467.1:c.606C= ENSP00000513325.1:p.Ser202=
ENST00000697468.1:c.678C= ENSP00000513326.1:p.Ser226=
ENST00000697469.1:c.387C= ENSP00000513327.1:p.Ser129=
ENST00000697470.1:c.291C= ENSP00000513328.1:p.Ser97=
ENST00000697557.1:c.678C= ENSP00000513335.1:p.Ser226=
ENST00000521381.6:c.1695C= MANE Select ENSP00000428056.1:p.Ser565=
ENST00000320694.12:c.795C= ENSP00000323512.8:p.Ser265=
ENST00000336483.9:c.885C= ENSP00000338554.5:p.Ser295=
ENST00000517698.5:c.*665C= ENSP00000430424.1:n.*665C=
ENST00000518813.5:n.2238C=
ENST00000520550.1:n.1094C=
ENST00000521381.5:c.1695C= ENSP00000428056.1:p.Ser565=
ENST00000521657.5:c.1695C= ENSP00000429277.1:p.Ser565=
ENST00000523872.1:c.606C= ENSP00000430098.1:p.Ser202=
NM_001242466.1:c.606C= NP_001229395.1:p.Ser202=
NM_181504.3:c.885C= NP_852556.2:p.Ser295=
NM_181523.2:c.1695C= NP_852664.1:p.Ser565=
NM_181524.1:c.795C= NP_852665.1:p.Ser265=
XM_005248542.2:c.1695C= XP_005248599.1:p.Ser565=
XM_011543493.1:c.1368C= XP_011541795.1:p.Ser456=
XM_005248542.3:c.1695C= XP_005248599.1:p.Ser565=
XM_011543493.3:c.1368C= XP_011541795.1:p.Ser456=
XM_017009585.2:c.1695C= XP_016865074.1:p.Ser565=
XM_017009586.1:c.1422C= XP_016865075.1:p.Ser474=
NM_181523.3:c.1695C= MANE Select NP_852664.1:p.Ser565=
NM_001242466.2:c.606C= NP_001229395.1:p.Ser202=
NM_181504.4:c.885C= NP_852556.2:p.Ser295=
NM_181524.2:c.795C= NP_852665.1:p.Ser265=