Canonical Allele Identifier: CA1553406192

Gene: PIK3R1

Linked Data

• dbSNP Id: rs1747650260

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.68295343A>G , CM000667.2:g.68295343A>G	GRCh38
NC_000005.9:g.67591171A>G , CM000667.1:g.67591171A>G	GRCh37
NC_000005.8:g.67626927A>G	NCBI36
NG_012849.2:g.84588A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320694.13:c.845+19A>G	ENSP00000323512.8:n.845+19A>G
ENST00000336483.10:c.935+19A>G	ENSP00000338554.5:n.935+19A>G
ENST00000517643.2:c.1745+19A>G	ENSP00000513333.1:n.1745+19A>G
ENST00000517698.6:c.*715+19A>G	ENSP00000430424.1:n.*715+19A>G
ENST00000521657.6:c.1745+19A>G	ENSP00000429277.1:n.1745+19A>G
ENST00000522084.6:c.935+19A>G	ENSP00000429766.2:n.935+19A>G
ENST00000697457.1:c.1670+19A>G	ENSP00000513315.1:n.1670+19A>G
ENST00000697458.1:c.1745+19A>G	ENSP00000513316.1:n.1745+19A>G
ENST00000697460.1:c.1220+19A>G	ENSP00000513318.1:n.1220+19A>G
ENST00000697461.1:c.1745+19A>G	ENSP00000513319.1:n.1745+19A>G
ENST00000697462.1:c.935+19A>G	ENSP00000513320.1:n.935+19A>G
ENST00000697463.1:n.1386+19A>G
ENST00000697464.1:c.*711+19A>G	ENSP00000513322.1:n.*711+19A>G
ENST00000697465.1:c.782+19A>G	ENSP00000513323.1:n.782+19A>G
ENST00000697466.1:c.752+19A>G	ENSP00000513324.1:n.752+19A>G
ENST00000697467.1:c.656+19A>G	ENSP00000513325.1:n.656+19A>G
ENST00000697468.1:c.728+19A>G	ENSP00000513326.1:n.728+19A>G
ENST00000697469.1:c.437+19A>G	ENSP00000513327.1:n.437+19A>G
ENST00000697470.1:c.341+19A>G	ENSP00000513328.1:n.341+19A>G
ENST00000697557.1:c.728+19A>G	ENSP00000513335.1:n.728+19A>G
ENST00000521381.6:c.1745+19A>G MANE Select	ENSP00000428056.1:n.1745+19A>G
ENST00000320694.12:c.845+19A>G	ENSP00000323512.8:n.845+19A>G
ENST00000336483.9:c.935+19A>G	ENSP00000338554.5:n.935+19A>G
ENST00000517698.5:c.*715+19A>G	ENSP00000430424.1:n.*715+19A>G
ENST00000518813.5:n.2288+19A>G
ENST00000520550.1:n.1144+19A>G
ENST00000521381.5:c.1745+19A>G	ENSP00000428056.1:n.1745+19A>G
ENST00000521657.5:c.1745+19A>G	ENSP00000429277.1:n.1745+19A>G
ENST00000523872.1:c.656+19A>G	ENSP00000430098.1:n.656+19A>G
NM_001242466.1:c.656+19A>G	NP_001229395.1:n.656+19A>G
NM_181504.3:c.935+19A>G	NP_852556.2:n.935+19A>G
NM_181523.2:c.1745+19A>G	NP_852664.1:n.1745+19A>G
NM_181524.1:c.845+19A>G	NP_852665.1:n.845+19A>G
XM_005248542.2:c.1745+19A>G	XP_005248599.1:n.1745+19A>G
XM_011543493.1:c.1418+19A>G	XP_011541795.1:n.1418+19A>G
XM_005248542.3:c.1745+19A>G	XP_005248599.1:n.1745+19A>G
XM_011543493.3:c.1418+19A>G	XP_011541795.1:n.1418+19A>G
XM_017009585.2:c.1745+19A>G	XP_016865074.1:n.1745+19A>G
XM_017009586.1:c.1472+19A>G	XP_016865075.1:n.1472+19A>G
NM_181523.3:c.1745+19A>G MANE Select	NP_852664.1:n.1745+19A>G
NM_001242466.2:c.656+19A>G	NP_001229395.1:n.656+19A>G
NM_181504.4:c.935+19A>G	NP_852556.2:n.935+19A>G
NM_181524.2:c.845+19A>G	NP_852665.1:n.845+19A>G