Canonical Allele Identifier: CA359882525

Gene: PIK3R1

Linked Data

• MyVariant Identifiers: chr5:g.67590990A>G (hg19) ; chr5:g.68295162A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.68295162A>G , CM000667.2:g.68295162A>G	GRCh38
NC_000005.9:g.67590990A>G , CM000667.1:g.67590990A>G	GRCh37
NC_000005.8:g.67626746A>G	NCBI36
NG_012849.2:g.84407A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320694.13:c.683A>G	ENSP00000323512.8:p.Tyr228Cys
ENST00000336483.10:c.773A>G	ENSP00000338554.5:p.Tyr258Cys
ENST00000517643.2:c.1583A>G	ENSP00000513333.1:p.Tyr528Cys
ENST00000517698.6:c.*553A>G	ENSP00000430424.1:n.*553A>G
ENST00000521657.6:c.1583A>G	ENSP00000429277.1:p.Tyr528Cys
ENST00000522084.6:c.773A>G	ENSP00000429766.2:p.Tyr258Cys
ENST00000697457.1:c.1508A>G	ENSP00000513315.1:p.Tyr503Cys
ENST00000697458.1:c.1583A>G	ENSP00000513316.1:p.Tyr528Cys
ENST00000697460.1:c.1058A>G	ENSP00000513318.1:p.Tyr353Cys
ENST00000697461.1:c.1583A>G	ENSP00000513319.1:p.Tyr528Cys
ENST00000697462.1:c.773A>G	ENSP00000513320.1:p.Tyr258Cys
ENST00000697463.1:n.1224A>G
ENST00000697464.1:c.*549A>G	ENSP00000513322.1:n.*549A>G
ENST00000697465.1:c.620A>G	ENSP00000513323.1:p.Tyr207Cys
ENST00000697466.1:c.590A>G	ENSP00000513324.1:p.Tyr197Cys
ENST00000697467.1:c.494A>G	ENSP00000513325.1:p.Tyr165Cys
ENST00000697468.1:c.566A>G	ENSP00000513326.1:p.Tyr189Cys
ENST00000697469.1:c.275A>G	ENSP00000513327.1:p.Tyr92Cys
ENST00000697470.1:c.179A>G	ENSP00000513328.1:p.Tyr60Cys
ENST00000697557.1:c.566A>G	ENSP00000513335.1:p.Tyr189Cys
ENST00000521381.6:c.1583A>G MANE Select	ENSP00000428056.1:p.Tyr528Cys
ENST00000320694.12:c.683A>G	ENSP00000323512.8:p.Tyr228Cys
ENST00000336483.9:c.773A>G	ENSP00000338554.5:p.Tyr258Cys
ENST00000517698.5:c.*553A>G	ENSP00000430424.1:n.*553A>G
ENST00000518813.5:n.2126A>G
ENST00000520550.1:n.982A>G
ENST00000521381.5:c.1583A>G	ENSP00000428056.1:p.Tyr528Cys
ENST00000521657.5:c.1583A>G	ENSP00000429277.1:p.Tyr528Cys
ENST00000523872.1:c.494A>G	ENSP00000430098.1:p.Tyr165Cys
NM_001242466.1:c.494A>G	NP_001229395.1:p.Tyr165Cys
NM_181504.3:c.773A>G	NP_852556.2:p.Tyr258Cys
NM_181523.2:c.1583A>G	NP_852664.1:p.Tyr528Cys
NM_181524.1:c.683A>G	NP_852665.1:p.Tyr228Cys
XM_005248542.2:c.1583A>G	XP_005248599.1:p.Tyr528Cys
XM_011543493.1:c.1256A>G	XP_011541795.1:p.Tyr419Cys
XM_005248542.3:c.1583A>G	XP_005248599.1:p.Tyr528Cys
XM_011543493.3:c.1256A>G	XP_011541795.1:p.Tyr419Cys
XM_017009585.2:c.1583A>G	XP_016865074.1:p.Tyr528Cys
XM_017009586.1:c.1310A>G	XP_016865075.1:p.Tyr437Cys
NM_181523.3:c.1583A>G MANE Select	NP_852664.1:p.Tyr528Cys
NM_001242466.2:c.494A>G	NP_001229395.1:p.Tyr165Cys
NM_181504.4:c.773A>G	NP_852556.2:p.Tyr258Cys
NM_181524.2:c.683A>G	NP_852665.1:p.Tyr228Cys