Canonical Allele Identifier: CA359883037

Gene: PIK3R1

Linked Data

• dbSNP Id: rs1057519841
• MyVariant Identifiers: chr5:g.67591097A>T (hg19) ; chr5:g.68295269A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.68295269A>T , CM000667.2:g.68295269A>T	GRCh38
NC_000005.9:g.67591097A>T , CM000667.1:g.67591097A>T	GRCh37
NC_000005.8:g.67626853A>T	NCBI36
NG_012849.2:g.84514A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000320694.13:c.790A>T	ENSP00000323512.8:p.Asn264Tyr
ENST00000336483.10:c.880A>T	ENSP00000338554.5:p.Asn294Tyr
ENST00000517643.2:c.1690A>T	ENSP00000513333.1:p.Asn564Tyr
ENST00000517698.6:c.*660A>T	ENSP00000430424.1:n.*660A>T
ENST00000521657.6:c.1690A>T	ENSP00000429277.1:p.Asn564Tyr
ENST00000522084.6:c.880A>T	ENSP00000429766.2:p.Asn294Tyr
ENST00000697457.1:c.1615A>T	ENSP00000513315.1:p.Asn539Tyr
ENST00000697458.1:c.1690A>T	ENSP00000513316.1:p.Asn564Tyr
ENST00000697460.1:c.1165A>T	ENSP00000513318.1:p.Asn389Tyr
ENST00000697461.1:c.1690A>T	ENSP00000513319.1:p.Asn564Tyr
ENST00000697462.1:c.880A>T	ENSP00000513320.1:p.Asn294Tyr
ENST00000697463.1:n.1331A>T
ENST00000697464.1:c.*656A>T	ENSP00000513322.1:n.*656A>T
ENST00000697465.1:c.727A>T	ENSP00000513323.1:p.Asn243Tyr
ENST00000697466.1:c.697A>T	ENSP00000513324.1:p.Asn233Tyr
ENST00000697467.1:c.601A>T	ENSP00000513325.1:p.Asn201Tyr
ENST00000697468.1:c.673A>T	ENSP00000513326.1:p.Asn225Tyr
ENST00000697469.1:c.382A>T	ENSP00000513327.1:p.Asn128Tyr
ENST00000697470.1:c.286A>T	ENSP00000513328.1:p.Asn96Tyr
ENST00000697557.1:c.673A>T	ENSP00000513335.1:p.Asn225Tyr
ENST00000521381.6:c.1690A>T MANE Select	ENSP00000428056.1:p.Asn564Tyr
ENST00000320694.12:c.790A>T	ENSP00000323512.8:p.Asn264Tyr
ENST00000336483.9:c.880A>T	ENSP00000338554.5:p.Asn294Tyr
ENST00000517698.5:c.*660A>T	ENSP00000430424.1:n.*660A>T
ENST00000518813.5:n.2233A>T
ENST00000520550.1:n.1089A>T
ENST00000521381.5:c.1690A>T	ENSP00000428056.1:p.Asn564Tyr
ENST00000521657.5:c.1690A>T	ENSP00000429277.1:p.Asn564Tyr
ENST00000523872.1:c.601A>T	ENSP00000430098.1:p.Asn201Tyr
NM_001242466.1:c.601A>T	NP_001229395.1:p.Asn201Tyr
NM_181504.3:c.880A>T	NP_852556.2:p.Asn294Tyr
NM_181523.2:c.1690A>T	NP_852664.1:p.Asn564Tyr
NM_181524.1:c.790A>T	NP_852665.1:p.Asn264Tyr
XM_005248542.2:c.1690A>T	XP_005248599.1:p.Asn564Tyr
XM_011543493.1:c.1363A>T	XP_011541795.1:p.Asn455Tyr
XM_005248542.3:c.1690A>T	XP_005248599.1:p.Asn564Tyr
XM_011543493.3:c.1363A>T	XP_011541795.1:p.Asn455Tyr
XM_017009585.2:c.1690A>T	XP_016865074.1:p.Asn564Tyr
XM_017009586.1:c.1417A>T	XP_016865075.1:p.Asn473Tyr
NM_181523.3:c.1690A>T MANE Select	NP_852664.1:p.Asn564Tyr
NM_001242466.2:c.601A>T	NP_001229395.1:p.Asn201Tyr
NM_181504.4:c.880A>T	NP_852556.2:p.Asn294Tyr
NM_181524.2:c.790A>T	NP_852665.1:p.Asn264Tyr