Canonical Allele Identifier: CA444672523

Gene: PIK3R1

Linked Data

• dbSNP Id: rs1747638275
• MyVariant Identifiers: chr5:g.67590997G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.68295169G>A , CM000667.2:g.68295169G>A	GRCh38
NC_000005.9:g.67590997G>A , CM000667.1:g.67590997G>A	GRCh37
NC_000005.8:g.67626753G>A	NCBI36
NG_012849.2:g.84414G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320694.13:c.690G>A	ENSP00000323512.8:p.Lys230=
ENST00000336483.10:c.780G>A	ENSP00000338554.5:p.Lys260=
ENST00000517643.2:c.1590G>A	ENSP00000513333.1:p.Lys530=
ENST00000517698.6:c.*560G>A	ENSP00000430424.1:n.*560G>A
ENST00000521657.6:c.1590G>A	ENSP00000429277.1:p.Lys530=
ENST00000522084.6:c.780G>A	ENSP00000429766.2:p.Lys260=
ENST00000697457.1:c.1515G>A	ENSP00000513315.1:p.Lys505=
ENST00000697458.1:c.1590G>A	ENSP00000513316.1:p.Lys530=
ENST00000697460.1:c.1065G>A	ENSP00000513318.1:p.Lys355=
ENST00000697461.1:c.1590G>A	ENSP00000513319.1:p.Lys530=
ENST00000697462.1:c.780G>A	ENSP00000513320.1:p.Lys260=
ENST00000697463.1:n.1231G>A
ENST00000697464.1:c.*556G>A	ENSP00000513322.1:n.*556G>A
ENST00000697465.1:c.627G>A	ENSP00000513323.1:p.Lys209=
ENST00000697466.1:c.597G>A	ENSP00000513324.1:p.Lys199=
ENST00000697467.1:c.501G>A	ENSP00000513325.1:p.Lys167=
ENST00000697468.1:c.573G>A	ENSP00000513326.1:p.Lys191=
ENST00000697469.1:c.282G>A	ENSP00000513327.1:p.Lys94=
ENST00000697470.1:c.186G>A	ENSP00000513328.1:p.Lys62=
ENST00000697557.1:c.573G>A	ENSP00000513335.1:p.Lys191=
ENST00000521381.6:c.1590G>A MANE Select	ENSP00000428056.1:p.Lys530=
ENST00000320694.12:c.690G>A	ENSP00000323512.8:p.Lys230=
ENST00000336483.9:c.780G>A	ENSP00000338554.5:p.Lys260=
ENST00000517698.5:c.*560G>A	ENSP00000430424.1:n.*560G>A
ENST00000518813.5:n.2133G>A
ENST00000520550.1:n.989G>A
ENST00000521381.5:c.1590G>A	ENSP00000428056.1:p.Lys530=
ENST00000521657.5:c.1590G>A	ENSP00000429277.1:p.Lys530=
ENST00000523872.1:c.501G>A	ENSP00000430098.1:p.Lys167=
NM_001242466.1:c.501G>A	NP_001229395.1:p.Lys167=
NM_181504.3:c.780G>A	NP_852556.2:p.Lys260=
NM_181523.2:c.1590G>A	NP_852664.1:p.Lys530=
NM_181524.1:c.690G>A	NP_852665.1:p.Lys230=
XM_005248542.2:c.1590G>A	XP_005248599.1:p.Lys530=
XM_011543493.1:c.1263G>A	XP_011541795.1:p.Lys421=
XM_005248542.3:c.1590G>A	XP_005248599.1:p.Lys530=
XM_011543493.3:c.1263G>A	XP_011541795.1:p.Lys421=
XM_017009585.2:c.1590G>A	XP_016865074.1:p.Lys530=
XM_017009586.1:c.1317G>A	XP_016865075.1:p.Lys439=
NM_181523.3:c.1590G>A MANE Select	NP_852664.1:p.Lys530=
NM_001242466.2:c.501G>A	NP_001229395.1:p.Lys167=
NM_181504.4:c.780G>A	NP_852556.2:p.Lys260=
NM_181524.2:c.690G>A	NP_852665.1:p.Lys230=