Canonical Allele Identifier: CA1553406164

Gene: PIK3R1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.68295257G= , CM000667.2:g.68295257G=	GRCh38
NC_000005.9:g.67591085G= , CM000667.1:g.67591085G=	GRCh37
NC_000005.8:g.67626841G=	NCBI36
NG_012849.2:g.84502G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320694.13:c.778G=	ENSP00000323512.8:p.Asp260=
ENST00000336483.10:c.868G=	ENSP00000338554.5:p.Asp290=
ENST00000517643.2:c.1678G=	ENSP00000513333.1:p.Asp560=
ENST00000517698.6:c.*648G=	ENSP00000430424.1:n.*648G=
ENST00000521657.6:c.1678G=	ENSP00000429277.1:p.Asp560=
ENST00000522084.6:c.868G=	ENSP00000429766.2:p.Asp290=
ENST00000697457.1:c.1603G=	ENSP00000513315.1:p.Asp535=
ENST00000697458.1:c.1678G=	ENSP00000513316.1:p.Asp560=
ENST00000697460.1:c.1153G=	ENSP00000513318.1:p.Asp385=
ENST00000697461.1:c.1678G=	ENSP00000513319.1:p.Asp560=
ENST00000697462.1:c.868G=	ENSP00000513320.1:p.Asp290=
ENST00000697463.1:n.1319G=
ENST00000697464.1:c.*644G=	ENSP00000513322.1:n.*644G=
ENST00000697465.1:c.715G=	ENSP00000513323.1:p.Asp239=
ENST00000697466.1:c.685G=	ENSP00000513324.1:p.Asp229=
ENST00000697467.1:c.589G=	ENSP00000513325.1:p.Asp197=
ENST00000697468.1:c.661G=	ENSP00000513326.1:p.Asp221=
ENST00000697469.1:c.370G=	ENSP00000513327.1:p.Asp124=
ENST00000697470.1:c.274G=	ENSP00000513328.1:p.Asp92=
ENST00000697557.1:c.661G=	ENSP00000513335.1:p.Asp221=
ENST00000521381.6:c.1678G= MANE Select	ENSP00000428056.1:p.Asp560=
ENST00000320694.12:c.778G=	ENSP00000323512.8:p.Asp260=
ENST00000336483.9:c.868G=	ENSP00000338554.5:p.Asp290=
ENST00000517698.5:c.*648G=	ENSP00000430424.1:n.*648G=
ENST00000518813.5:n.2221G=
ENST00000520550.1:n.1077G=
ENST00000521381.5:c.1678G=	ENSP00000428056.1:p.Asp560=
ENST00000521657.5:c.1678G=	ENSP00000429277.1:p.Asp560=
ENST00000523872.1:c.589G=	ENSP00000430098.1:p.Asp197=
NM_001242466.1:c.589G=	NP_001229395.1:p.Asp197=
NM_181504.3:c.868G=	NP_852556.2:p.Asp290=
NM_181523.2:c.1678G=	NP_852664.1:p.Asp560=
NM_181524.1:c.778G=	NP_852665.1:p.Asp260=
XM_005248542.2:c.1678G=	XP_005248599.1:p.Asp560=
XM_011543493.1:c.1351G=	XP_011541795.1:p.Asp451=
XM_005248542.3:c.1678G=	XP_005248599.1:p.Asp560=
XM_011543493.3:c.1351G=	XP_011541795.1:p.Asp451=
XM_017009585.2:c.1678G=	XP_016865074.1:p.Asp560=
XM_017009586.1:c.1405G=	XP_016865075.1:p.Asp469=
NM_181523.3:c.1678G= MANE Select	NP_852664.1:p.Asp560=
NM_001242466.2:c.589G=	NP_001229395.1:p.Asp197=
NM_181504.4:c.868G=	NP_852556.2:p.Asp290=
NM_181524.2:c.778G=	NP_852665.1:p.Asp260=