Canonical Allele Identifier: CA1553406627

Gene: PIK3R1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.68296301C= , CM000667.2:g.68296301C=	GRCh38
NC_000005.9:g.67592129C= , CM000667.1:g.67592129C=	GRCh37
NC_000005.8:g.67627885C=	NCBI36
NG_012849.2:g.85546C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320694.13:c.1045C=	ENSP00000323512.8:p.Arg349=
ENST00000336483.10:c.1135C=	ENSP00000338554.5:p.Arg379=
ENST00000517643.2:c.1945C=	ENSP00000513333.1:p.Arg649=
ENST00000517698.6:c.*915C=	ENSP00000430424.1:n.*915C=
ENST00000521657.6:c.1945C=	ENSP00000429277.1:p.Arg649=
ENST00000522084.6:c.1135C=	ENSP00000429766.2:p.Arg379=
ENST00000697457.1:c.1870C=	ENSP00000513315.1:p.Arg624=
ENST00000697458.1:c.1945C=	ENSP00000513316.1:p.Arg649=
ENST00000697460.1:c.1420C=	ENSP00000513318.1:p.Arg474=
ENST00000697461.1:c.1969C=	ENSP00000513319.1:p.Arg657=
ENST00000697462.1:c.1159C=	ENSP00000513320.1:p.Arg387=
ENST00000697463.1:n.1610C=
ENST00000697464.1:c.*911C=	ENSP00000513322.1:n.*911C=
ENST00000697465.1:c.982C=	ENSP00000513323.1:p.Arg328=
ENST00000697466.1:c.952C=	ENSP00000513324.1:p.Arg318=
ENST00000697467.1:c.856C=	ENSP00000513325.1:p.Arg286=
ENST00000697468.1:c.928C=	ENSP00000513326.1:p.Arg310=
ENST00000697469.1:c.637C=	ENSP00000513327.1:p.Arg213=
ENST00000697470.1:c.541C=	ENSP00000513328.1:p.Arg181=
ENST00000697557.1:c.928C=	ENSP00000513335.1:p.Arg310=
ENST00000521381.6:c.1945C= MANE Select	ENSP00000428056.1:p.Arg649=
ENST00000320694.12:c.1045C=	ENSP00000323512.8:p.Arg349=
ENST00000336483.9:c.1135C=	ENSP00000338554.5:p.Arg379=
ENST00000518813.5:n.2488C=
ENST00000521381.5:c.1945C=	ENSP00000428056.1:p.Arg649=
ENST00000521657.5:c.1945C=	ENSP00000429277.1:p.Arg649=
ENST00000523872.1:c.856C=	ENSP00000430098.1:p.Arg286=
NM_001242466.1:c.856C=	NP_001229395.1:p.Arg286=
NM_181504.3:c.1135C=	NP_852556.2:p.Arg379=
NM_181523.2:c.1945C=	NP_852664.1:p.Arg649=
NM_181524.1:c.1045C=	NP_852665.1:p.Arg349=
XM_005248542.2:c.1945C=	XP_005248599.1:p.Arg649=
XM_011543493.1:c.1618C=	XP_011541795.1:p.Arg540=
XM_005248542.3:c.1945C=	XP_005248599.1:p.Arg649=
XM_011543493.3:c.1618C=	XP_011541795.1:p.Arg540=
XM_017009585.2:c.1945C=	XP_016865074.1:p.Arg649=
XM_017009586.1:c.1672C=	XP_016865075.1:p.Arg558=
NM_181523.3:c.1945C= MANE Select	NP_852664.1:p.Arg649=
NM_001242466.2:c.856C=	NP_001229395.1:p.Arg286=
NM_181504.4:c.1135C=	NP_852556.2:p.Arg379=
NM_181524.2:c.1045C=	NP_852665.1:p.Arg349=