Canonical Allele Identifier: CA1553406604

Gene: PIK3R1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.68296248G= , CM000667.2:g.68296248G=	GRCh38
NC_000005.9:g.67592076G= , CM000667.1:g.67592076G=	GRCh37
NC_000005.8:g.67627832G=	NCBI36
NG_012849.2:g.85493G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320694.13:c.992G=	ENSP00000323512.8:p.Arg331=
ENST00000336483.10:c.1082G=	ENSP00000338554.5:p.Arg361=
ENST00000517643.2:c.1892G=	ENSP00000513333.1:p.Arg631=
ENST00000517698.6:c.*862G=	ENSP00000430424.1:n.*862G=
ENST00000521657.6:c.1892G=	ENSP00000429277.1:p.Arg631=
ENST00000522084.6:c.1082G=	ENSP00000429766.2:p.Arg361=
ENST00000697457.1:c.1817G=	ENSP00000513315.1:p.Arg606=
ENST00000697458.1:c.1892G=	ENSP00000513316.1:p.Arg631=
ENST00000697460.1:c.1367G=	ENSP00000513318.1:p.Arg456=
ENST00000697461.1:c.1916G=	ENSP00000513319.1:p.Arg639=
ENST00000697462.1:c.1106G=	ENSP00000513320.1:p.Arg369=
ENST00000697463.1:n.1557G=
ENST00000697464.1:c.*858G=	ENSP00000513322.1:n.*858G=
ENST00000697465.1:c.929G=	ENSP00000513323.1:p.Arg310=
ENST00000697466.1:c.899G=	ENSP00000513324.1:p.Arg300=
ENST00000697467.1:c.803G=	ENSP00000513325.1:p.Arg268=
ENST00000697468.1:c.875G=	ENSP00000513326.1:p.Arg292=
ENST00000697469.1:c.584G=	ENSP00000513327.1:p.Arg195=
ENST00000697470.1:c.488G=	ENSP00000513328.1:p.Arg163=
ENST00000697557.1:c.875G=	ENSP00000513335.1:p.Arg292=
ENST00000521381.6:c.1892G= MANE Select	ENSP00000428056.1:p.Arg631=
ENST00000320694.12:c.992G=	ENSP00000323512.8:p.Arg331=
ENST00000336483.9:c.1082G=	ENSP00000338554.5:p.Arg361=
ENST00000518813.5:n.2435G=
ENST00000521381.5:c.1892G=	ENSP00000428056.1:p.Arg631=
ENST00000521657.5:c.1892G=	ENSP00000429277.1:p.Arg631=
ENST00000523872.1:c.803G=	ENSP00000430098.1:p.Arg268=
NM_001242466.1:c.803G=	NP_001229395.1:p.Arg268=
NM_181504.3:c.1082G=	NP_852556.2:p.Arg361=
NM_181523.2:c.1892G=	NP_852664.1:p.Arg631=
NM_181524.1:c.992G=	NP_852665.1:p.Arg331=
XM_005248542.2:c.1892G=	XP_005248599.1:p.Arg631=
XM_011543493.1:c.1565G=	XP_011541795.1:p.Arg522=
XM_005248542.3:c.1892G=	XP_005248599.1:p.Arg631=
XM_011543493.3:c.1565G=	XP_011541795.1:p.Arg522=
XM_017009585.2:c.1892G=	XP_016865074.1:p.Arg631=
XM_017009586.1:c.1619G=	XP_016865075.1:p.Arg540=
NM_181523.3:c.1892G= MANE Select	NP_852664.1:p.Arg631=
NM_001242466.2:c.803G=	NP_001229395.1:p.Arg268=
NM_181504.4:c.1082G=	NP_852556.2:p.Arg361=
NM_181524.2:c.992G=	NP_852665.1:p.Arg331=