Canonical Allele Identifier: CA347796

Gene: PIK3R1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320694.13:c.992G>A	ENSP00000323512.8:p.Arg331Gln
ENST00000336483.10:c.1082G>A	ENSP00000338554.5:p.Arg361Gln
ENST00000517643.2:c.1892G>A	ENSP00000513333.1:p.Arg631Gln
ENST00000517698.6:c.*862G>A	ENSP00000430424.1:n.*862G>A
ENST00000521657.6:c.1892G>A	ENSP00000429277.1:p.Arg631Gln
ENST00000522084.6:c.1082G>A	ENSP00000429766.2:p.Arg361Gln
ENST00000697457.1:c.1817G>A	ENSP00000513315.1:p.Arg606Gln
ENST00000697458.1:c.1892G>A	ENSP00000513316.1:p.Arg631Gln
ENST00000697460.1:c.1367G>A	ENSP00000513318.1:p.Arg456Gln
ENST00000697461.1:c.1916G>A	ENSP00000513319.1:p.Arg639Gln
ENST00000697462.1:c.1106G>A	ENSP00000513320.1:p.Arg369Gln
ENST00000697463.1:n.1557G>A
ENST00000697464.1:c.*858G>A	ENSP00000513322.1:n.*858G>A
ENST00000697465.1:c.929G>A	ENSP00000513323.1:p.Arg310Gln
ENST00000697466.1:c.899G>A	ENSP00000513324.1:p.Arg300Gln
ENST00000697467.1:c.803G>A	ENSP00000513325.1:p.Arg268Gln
ENST00000697468.1:c.875G>A	ENSP00000513326.1:p.Arg292Gln
ENST00000697469.1:c.584G>A	ENSP00000513327.1:p.Arg195Gln
ENST00000697470.1:c.488G>A	ENSP00000513328.1:p.Arg163Gln
ENST00000697557.1:c.875G>A	ENSP00000513335.1:p.Arg292Gln
ENST00000521381.6:c.1892G>A MANE Select	ENSP00000428056.1:p.Arg631Gln
ENST00000320694.12:c.992G>A	ENSP00000323512.8:p.Arg331Gln
ENST00000336483.9:c.1082G>A	ENSP00000338554.5:p.Arg361Gln
ENST00000518813.5:n.2435G>A
ENST00000521381.5:c.1892G>A	ENSP00000428056.1:p.Arg631Gln
ENST00000521657.5:c.1892G>A	ENSP00000429277.1:p.Arg631Gln
ENST00000523872.1:c.803G>A	ENSP00000430098.1:p.Arg268Gln
NM_001242466.1:c.803G>A	NP_001229395.1:p.Arg268Gln
NM_181504.3:c.1082G>A	NP_852556.2:p.Arg361Gln
NM_181523.2:c.1892G>A	NP_852664.1:p.Arg631Gln
NM_181524.1:c.992G>A	NP_852665.1:p.Arg331Gln
XM_005248542.2:c.1892G>A	XP_005248599.1:p.Arg631Gln
XM_011543493.1:c.1565G>A	XP_011541795.1:p.Arg522Gln
XM_005248542.3:c.1892G>A	XP_005248599.1:p.Arg631Gln
XM_011543493.3:c.1565G>A	XP_011541795.1:p.Arg522Gln
XM_017009585.2:c.1892G>A	XP_016865074.1:p.Arg631Gln
XM_017009586.1:c.1619G>A	XP_016865075.1:p.Arg540Gln
NM_181523.3:c.1892G>A MANE Select	NP_852664.1:p.Arg631Gln
NM_001242466.2:c.803G>A	NP_001229395.1:p.Arg268Gln
NM_181504.4:c.1082G>A	NP_852556.2:p.Arg361Gln
NM_181524.2:c.992G>A	NP_852665.1:p.Arg331Gln