Canonical Allele Identifier: CA444672549

Gene: PIK3R1

Linked Data

• dbSNP Id: rs2112274513
• MyVariant Identifiers: chr5:g.67591009A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.68295181A>T , CM000667.2:g.68295181A>T	GRCh38
NC_000005.9:g.67591009A>T , CM000667.1:g.67591009A>T	GRCh37
NC_000005.8:g.67626765A>T	NCBI36
NG_012849.2:g.84426A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320694.13:c.702A>T	ENSP00000323512.8:p.Arg234=
ENST00000336483.10:c.792A>T	ENSP00000338554.5:p.Arg264=
ENST00000517643.2:c.1602A>T	ENSP00000513333.1:p.Arg534=
ENST00000517698.6:c.*572A>T	ENSP00000430424.1:n.*572A>T
ENST00000521657.6:c.1602A>T	ENSP00000429277.1:p.Arg534=
ENST00000522084.6:c.792A>T	ENSP00000429766.2:p.Arg264=
ENST00000697457.1:c.1527A>T	ENSP00000513315.1:p.Arg509=
ENST00000697458.1:c.1602A>T	ENSP00000513316.1:p.Arg534=
ENST00000697460.1:c.1077A>T	ENSP00000513318.1:p.Arg359=
ENST00000697461.1:c.1602A>T	ENSP00000513319.1:p.Arg534=
ENST00000697462.1:c.792A>T	ENSP00000513320.1:p.Arg264=
ENST00000697463.1:n.1243A>T
ENST00000697464.1:c.*568A>T	ENSP00000513322.1:n.*568A>T
ENST00000697465.1:c.639A>T	ENSP00000513323.1:p.Arg213=
ENST00000697466.1:c.609A>T	ENSP00000513324.1:p.Arg203=
ENST00000697467.1:c.513A>T	ENSP00000513325.1:p.Arg171=
ENST00000697468.1:c.585A>T	ENSP00000513326.1:p.Arg195=
ENST00000697469.1:c.294A>T	ENSP00000513327.1:p.Arg98=
ENST00000697470.1:c.198A>T	ENSP00000513328.1:p.Arg66=
ENST00000697557.1:c.585A>T	ENSP00000513335.1:p.Arg195=
ENST00000521381.6:c.1602A>T MANE Select	ENSP00000428056.1:p.Arg534=
ENST00000320694.12:c.702A>T	ENSP00000323512.8:p.Arg234=
ENST00000336483.9:c.792A>T	ENSP00000338554.5:p.Arg264=
ENST00000517698.5:c.*572A>T	ENSP00000430424.1:n.*572A>T
ENST00000518813.5:n.2145A>T
ENST00000520550.1:n.1001A>T
ENST00000521381.5:c.1602A>T	ENSP00000428056.1:p.Arg534=
ENST00000521657.5:c.1602A>T	ENSP00000429277.1:p.Arg534=
ENST00000523872.1:c.513A>T	ENSP00000430098.1:p.Arg171=
NM_001242466.1:c.513A>T	NP_001229395.1:p.Arg171=
NM_181504.3:c.792A>T	NP_852556.2:p.Arg264=
NM_181523.2:c.1602A>T	NP_852664.1:p.Arg534=
NM_181524.1:c.702A>T	NP_852665.1:p.Arg234=
XM_005248542.2:c.1602A>T	XP_005248599.1:p.Arg534=
XM_011543493.1:c.1275A>T	XP_011541795.1:p.Arg425=
XM_005248542.3:c.1602A>T	XP_005248599.1:p.Arg534=
XM_011543493.3:c.1275A>T	XP_011541795.1:p.Arg425=
XM_017009585.2:c.1602A>T	XP_016865074.1:p.Arg534=
XM_017009586.1:c.1329A>T	XP_016865075.1:p.Arg443=
NM_181523.3:c.1602A>T MANE Select	NP_852664.1:p.Arg534=
NM_001242466.2:c.513A>T	NP_001229395.1:p.Arg171=
NM_181504.4:c.792A>T	NP_852556.2:p.Arg264=
NM_181524.2:c.702A>T	NP_852665.1:p.Arg234=