Canonical Allele Identifier: CA359882639

Gene: PIK3R1

Linked Data

• dbSNP Id: rs1747638906
• MyVariant Identifiers: chr5:g.67591005C>T (hg19) ; chr5:g.68295177C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.68295177C>T , CM000667.2:g.68295177C>T	GRCh38
NC_000005.9:g.67591005C>T , CM000667.1:g.67591005C>T	GRCh37
NC_000005.8:g.67626761C>T	NCBI36
NG_012849.2:g.84422C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320694.13:c.698C>T	ENSP00000323512.8:p.Ser233Phe
ENST00000336483.10:c.788C>T	ENSP00000338554.5:p.Ser263Phe
ENST00000517643.2:c.1598C>T	ENSP00000513333.1:p.Ser533Phe
ENST00000517698.6:c.*568C>T	ENSP00000430424.1:n.*568C>T
ENST00000521657.6:c.1598C>T	ENSP00000429277.1:p.Ser533Phe
ENST00000522084.6:c.788C>T	ENSP00000429766.2:p.Ser263Phe
ENST00000697457.1:c.1523C>T	ENSP00000513315.1:p.Ser508Phe
ENST00000697458.1:c.1598C>T	ENSP00000513316.1:p.Ser533Phe
ENST00000697460.1:c.1073C>T	ENSP00000513318.1:p.Ser358Phe
ENST00000697461.1:c.1598C>T	ENSP00000513319.1:p.Ser533Phe
ENST00000697462.1:c.788C>T	ENSP00000513320.1:p.Ser263Phe
ENST00000697463.1:n.1239C>T
ENST00000697464.1:c.*564C>T	ENSP00000513322.1:n.*564C>T
ENST00000697465.1:c.635C>T	ENSP00000513323.1:p.Ser212Phe
ENST00000697466.1:c.605C>T	ENSP00000513324.1:p.Ser202Phe
ENST00000697467.1:c.509C>T	ENSP00000513325.1:p.Ser170Phe
ENST00000697468.1:c.581C>T	ENSP00000513326.1:p.Ser194Phe
ENST00000697469.1:c.290C>T	ENSP00000513327.1:p.Ser97Phe
ENST00000697470.1:c.194C>T	ENSP00000513328.1:p.Ser65Phe
ENST00000697557.1:c.581C>T	ENSP00000513335.1:p.Ser194Phe
ENST00000521381.6:c.1598C>T MANE Select	ENSP00000428056.1:p.Ser533Phe
ENST00000320694.12:c.698C>T	ENSP00000323512.8:p.Ser233Phe
ENST00000336483.9:c.788C>T	ENSP00000338554.5:p.Ser263Phe
ENST00000517698.5:c.*568C>T	ENSP00000430424.1:n.*568C>T
ENST00000518813.5:n.2141C>T
ENST00000520550.1:n.997C>T
ENST00000521381.5:c.1598C>T	ENSP00000428056.1:p.Ser533Phe
ENST00000521657.5:c.1598C>T	ENSP00000429277.1:p.Ser533Phe
ENST00000523872.1:c.509C>T	ENSP00000430098.1:p.Ser170Phe
NM_001242466.1:c.509C>T	NP_001229395.1:p.Ser170Phe
NM_181504.3:c.788C>T	NP_852556.2:p.Ser263Phe
NM_181523.2:c.1598C>T	NP_852664.1:p.Ser533Phe
NM_181524.1:c.698C>T	NP_852665.1:p.Ser233Phe
XM_005248542.2:c.1598C>T	XP_005248599.1:p.Ser533Phe
XM_011543493.1:c.1271C>T	XP_011541795.1:p.Ser424Phe
XM_005248542.3:c.1598C>T	XP_005248599.1:p.Ser533Phe
XM_011543493.3:c.1271C>T	XP_011541795.1:p.Ser424Phe
XM_017009585.2:c.1598C>T	XP_016865074.1:p.Ser533Phe
XM_017009586.1:c.1325C>T	XP_016865075.1:p.Ser442Phe
NM_181523.3:c.1598C>T MANE Select	NP_852664.1:p.Ser533Phe
NM_001242466.2:c.509C>T	NP_001229395.1:p.Ser170Phe
NM_181504.4:c.788C>T	NP_852556.2:p.Ser263Phe
NM_181524.2:c.698C>T	NP_852665.1:p.Ser233Phe