Canonical Allele Identifier: CA359883132

Gene: PIK3R1

Linked Data

• MyVariant Identifiers: chr5:g.67591139G>T (hg19) ; chr5:g.68295311G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.68295311G>T , CM000667.2:g.68295311G>T	GRCh38
NC_000005.9:g.67591139G>T , CM000667.1:g.67591139G>T	GRCh37
NC_000005.8:g.67626895G>T	NCBI36
NG_012849.2:g.84556G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000320694.13:c.832G>T	ENSP00000323512.8:p.Asp278Tyr
ENST00000336483.10:c.922G>T	ENSP00000338554.5:p.Asp308Tyr
ENST00000517643.2:c.1732G>T	ENSP00000513333.1:p.Asp578Tyr
ENST00000517698.6:c.*702G>T	ENSP00000430424.1:n.*702G>T
ENST00000521657.6:c.1732G>T	ENSP00000429277.1:p.Asp578Tyr
ENST00000522084.6:c.922G>T	ENSP00000429766.2:p.Asp308Tyr
ENST00000697457.1:c.1657G>T	ENSP00000513315.1:p.Asp553Tyr
ENST00000697458.1:c.1732G>T	ENSP00000513316.1:p.Asp578Tyr
ENST00000697460.1:c.1207G>T	ENSP00000513318.1:p.Asp403Tyr
ENST00000697461.1:c.1732G>T	ENSP00000513319.1:p.Asp578Tyr
ENST00000697462.1:c.922G>T	ENSP00000513320.1:p.Asp308Tyr
ENST00000697463.1:n.1373G>T
ENST00000697464.1:c.*698G>T	ENSP00000513322.1:n.*698G>T
ENST00000697465.1:c.769G>T	ENSP00000513323.1:p.Asp257Tyr
ENST00000697466.1:c.739G>T	ENSP00000513324.1:p.Asp247Tyr
ENST00000697467.1:c.643G>T	ENSP00000513325.1:p.Asp215Tyr
ENST00000697468.1:c.715G>T	ENSP00000513326.1:p.Asp239Tyr
ENST00000697469.1:c.424G>T	ENSP00000513327.1:p.Asp142Tyr
ENST00000697470.1:c.328G>T	ENSP00000513328.1:p.Asp110Tyr
ENST00000697557.1:c.715G>T	ENSP00000513335.1:p.Asp239Tyr
ENST00000521381.6:c.1732G>T MANE Select	ENSP00000428056.1:p.Asp578Tyr
ENST00000320694.12:c.832G>T	ENSP00000323512.8:p.Asp278Tyr
ENST00000336483.9:c.922G>T	ENSP00000338554.5:p.Asp308Tyr
ENST00000517698.5:c.*702G>T	ENSP00000430424.1:n.*702G>T
ENST00000518813.5:n.2275G>T
ENST00000520550.1:n.1131G>T
ENST00000521381.5:c.1732G>T	ENSP00000428056.1:p.Asp578Tyr
ENST00000521657.5:c.1732G>T	ENSP00000429277.1:p.Asp578Tyr
ENST00000523872.1:c.643G>T	ENSP00000430098.1:p.Asp215Tyr
NM_001242466.1:c.643G>T	NP_001229395.1:p.Asp215Tyr
NM_181504.3:c.922G>T	NP_852556.2:p.Asp308Tyr
NM_181523.2:c.1732G>T	NP_852664.1:p.Asp578Tyr
NM_181524.1:c.832G>T	NP_852665.1:p.Asp278Tyr
XM_005248542.2:c.1732G>T	XP_005248599.1:p.Asp578Tyr
XM_011543493.1:c.1405G>T	XP_011541795.1:p.Asp469Tyr
XM_005248542.3:c.1732G>T	XP_005248599.1:p.Asp578Tyr
XM_011543493.3:c.1405G>T	XP_011541795.1:p.Asp469Tyr
XM_017009585.2:c.1732G>T	XP_016865074.1:p.Asp578Tyr
XM_017009586.1:c.1459G>T	XP_016865075.1:p.Asp487Tyr
NM_181523.3:c.1732G>T MANE Select	NP_852664.1:p.Asp578Tyr
NM_001242466.2:c.643G>T	NP_001229395.1:p.Asp215Tyr
NM_181504.4:c.922G>T	NP_852556.2:p.Asp308Tyr
NM_181524.2:c.832G>T	NP_852665.1:p.Asp278Tyr