Canonical Allele Identifier: CA2674090506

Gene: PIK3R1

Linked Data

• gnomAD v4: 5-68295131-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.68295134dup , CM000667.2:g.68295134dup	GRCh38
NC_000005.9:g.67590962dup , CM000667.1:g.67590962dup	GRCh37
NC_000005.8:g.67626718dup	NCBI36
NG_012849.2:g.84379dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320694.13:c.669-14dup	ENSP00000323512.8:n.669-14dup
ENST00000336483.10:c.759-14dup	ENSP00000338554.5:n.759-14dup
ENST00000517643.2:c.1569-14dup	ENSP00000513333.1:n.1569-14dup
ENST00000517698.6:c.*539-14dup	ENSP00000430424.1:n.*539-14dup
ENST00000521657.6:c.1569-14dup	ENSP00000429277.1:n.1569-14dup
ENST00000522084.6:c.759-14dup	ENSP00000429766.2:n.759-14dup
ENST00000697457.1:c.1494-14dup	ENSP00000513315.1:n.1494-14dup
ENST00000697458.1:c.1569-14dup	ENSP00000513316.1:n.1569-14dup
ENST00000697460.1:c.1044-14dup	ENSP00000513318.1:n.1044-14dup
ENST00000697461.1:c.1569-14dup	ENSP00000513319.1:n.1569-14dup
ENST00000697462.1:c.759-14dup	ENSP00000513320.1:n.759-14dup
ENST00000697463.1:n.1210-14dup
ENST00000697464.1:c.*535-14dup	ENSP00000513322.1:n.*535-14dup
ENST00000697465.1:c.606-14dup	ENSP00000513323.1:n.606-14dup
ENST00000697466.1:c.576-14dup	ENSP00000513324.1:n.576-14dup
ENST00000697467.1:c.480-14dup	ENSP00000513325.1:n.480-14dup
ENST00000697468.1:c.552-14dup	ENSP00000513326.1:n.552-14dup
ENST00000697469.1:c.261-14dup	ENSP00000513327.1:n.261-14dup
ENST00000697470.1:c.165-14dup	ENSP00000513328.1:n.165-14dup
ENST00000697557.1:c.552-14dup	ENSP00000513335.1:n.552-14dup
ENST00000521381.6:c.1569-14dup MANE Select	ENSP00000428056.1:n.1569-14dup
ENST00000320694.12:c.669-14dup	ENSP00000323512.8:n.669-14dup
ENST00000336483.9:c.759-14dup	ENSP00000338554.5:n.759-14dup
ENST00000517698.5:c.*539-14dup	ENSP00000430424.1:n.*539-14dup
ENST00000518813.5:n.2112-14dup
ENST00000520550.1:n.968-14dup
ENST00000521381.5:c.1569-14dup	ENSP00000428056.1:n.1569-14dup
ENST00000521657.5:c.1569-14dup	ENSP00000429277.1:n.1569-14dup
ENST00000523872.1:c.480-14dup	ENSP00000430098.1:n.480-14dup
NM_001242466.1:c.480-14dup	NP_001229395.1:n.480-14dup
NM_181504.3:c.759-14dup	NP_852556.2:n.759-14dup
NM_181523.2:c.1569-14dup	NP_852664.1:n.1569-14dup
NM_181524.1:c.669-14dup	NP_852665.1:n.669-14dup
XM_005248542.2:c.1569-14dup	XP_005248599.1:n.1569-14dup
XM_011543493.1:c.1242-14dup	XP_011541795.1:n.1242-14dup
XM_005248542.3:c.1569-14dup	XP_005248599.1:n.1569-14dup
XM_011543493.3:c.1242-14dup	XP_011541795.1:n.1242-14dup
XM_017009585.2:c.1569-14dup	XP_016865074.1:n.1569-14dup
XM_017009586.1:c.1296-14dup	XP_016865075.1:n.1296-14dup
NM_181523.3:c.1569-14dup MANE Select	NP_852664.1:n.1569-14dup
NM_001242466.2:c.480-14dup	NP_001229395.1:n.480-14dup
NM_181504.4:c.759-14dup	NP_852556.2:n.759-14dup
NM_181524.2:c.669-14dup	NP_852665.1:n.669-14dup