Canonical Allele Identifier: CA1553405267

Gene: PIK3R1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.68293310G= , CM000667.2:g.68293310G=	GRCh38
NC_000005.9:g.67589138G= , CM000667.1:g.67589138G=	GRCh37
NC_000005.8:g.67624894G=	NCBI36
NG_012849.2:g.82555G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320694.13:c.226G=	ENSP00000323512.8:p.Gly76=
ENST00000336483.10:c.316G=	ENSP00000338554.5:p.Gly106=
ENST00000517643.2:c.1126G=	ENSP00000513333.1:p.Gly376=
ENST00000517698.6:c.*96G=	ENSP00000430424.1:n.*96G=
ENST00000521657.6:c.1126G=	ENSP00000429277.1:p.Gly376=
ENST00000522084.6:c.316G=	ENSP00000429766.2:p.Gly106=
ENST00000697457.1:c.1051G=	ENSP00000513315.1:p.Gly351=
ENST00000697458.1:c.1126G=	ENSP00000513316.1:p.Gly376=
ENST00000697460.1:c.601G=	ENSP00000513318.1:p.Gly201=
ENST00000697461.1:c.1126G=	ENSP00000513319.1:p.Gly376=
ENST00000697462.1:c.316G=	ENSP00000513320.1:p.Gly106=
ENST00000697463.1:n.767G=
ENST00000697464.1:c.*92G=	ENSP00000513322.1:n.*92G=
ENST00000697465.1:c.163G=	ENSP00000513323.1:p.Gly55=
ENST00000697466.1:c.133G=	ENSP00000513324.1:p.Gly45=
ENST00000697467.1:c.37G=	ENSP00000513325.1:p.Gly13=
ENST00000697468.1:c.109G=	ENSP00000513326.1:p.Gly37=
ENST00000697556.1:c.1033G=	ENSP00000513334.1:p.Gly345=
ENST00000697557.1:c.109G=	ENSP00000513335.1:p.Gly37=
ENST00000521381.6:c.1126G= MANE Select	ENSP00000428056.1:p.Gly376=
ENST00000320694.12:c.226G=	ENSP00000323512.8:p.Gly76=
ENST00000336483.9:c.316G=	ENSP00000338554.5:p.Gly106=
ENST00000517698.5:c.*96G=	ENSP00000430424.1:n.*96G=
ENST00000518292.1:n.476G=
ENST00000518813.5:n.1669G=
ENST00000519025.5:c.145G=	ENSP00000429156.1:p.Gly49=
ENST00000520550.1:n.525G=
ENST00000521381.5:c.1126G=	ENSP00000428056.1:p.Gly376=
ENST00000521409.5:c.37G=	ENSP00000431058.1:p.Gly13=
ENST00000521657.5:c.1126G=	ENSP00000429277.1:p.Gly376=
ENST00000523807.5:c.316G=	ENSP00000430126.1:p.Gly106=
ENST00000523872.1:c.37G=	ENSP00000430098.1:p.Gly13=
NM_001242466.1:c.37G=	NP_001229395.1:p.Gly13=
NM_181504.3:c.316G=	NP_852556.2:p.Gly106=
NM_181523.2:c.1126G=	NP_852664.1:p.Gly376=
NM_181524.1:c.226G=	NP_852665.1:p.Gly76=
XM_005248542.2:c.1126G=	XP_005248599.1:p.Gly376=
XM_011543493.1:c.799G=	XP_011541795.1:p.Gly267=
XM_005248542.3:c.1126G=	XP_005248599.1:p.Gly376=
XM_011543493.3:c.799G=	XP_011541795.1:p.Gly267=
XM_017009585.2:c.1126G=	XP_016865074.1:p.Gly376=
XM_017009586.1:c.853G=	XP_016865075.1:p.Gly285=
NM_181523.3:c.1126G= MANE Select	NP_852664.1:p.Gly376=
NM_001242466.2:c.37G=	NP_001229395.1:p.Gly13=
NM_181504.4:c.316G=	NP_852556.2:p.Gly106=
NM_181524.2:c.226G=	NP_852665.1:p.Gly76=