Canonical Allele Identifier: CA359883135

Gene: PIK3R1

Linked Data

• MyVariant Identifiers: chr5:g.67591140A>C (hg19) ; chr5:g.68295312A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.68295312A>C , CM000667.2:g.68295312A>C	GRCh38
NC_000005.9:g.67591140A>C , CM000667.1:g.67591140A>C	GRCh37
NC_000005.8:g.67626896A>C	NCBI36
NG_012849.2:g.84557A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000320694.13:c.833A>C	ENSP00000323512.8:p.Asp278Ala
ENST00000336483.10:c.923A>C	ENSP00000338554.5:p.Asp308Ala
ENST00000517643.2:c.1733A>C	ENSP00000513333.1:p.Asp578Ala
ENST00000517698.6:c.*703A>C	ENSP00000430424.1:n.*703A>C
ENST00000521657.6:c.1733A>C	ENSP00000429277.1:p.Asp578Ala
ENST00000522084.6:c.923A>C	ENSP00000429766.2:p.Asp308Ala
ENST00000697457.1:c.1658A>C	ENSP00000513315.1:p.Asp553Ala
ENST00000697458.1:c.1733A>C	ENSP00000513316.1:p.Asp578Ala
ENST00000697460.1:c.1208A>C	ENSP00000513318.1:p.Asp403Ala
ENST00000697461.1:c.1733A>C	ENSP00000513319.1:p.Asp578Ala
ENST00000697462.1:c.923A>C	ENSP00000513320.1:p.Asp308Ala
ENST00000697463.1:n.1374A>C
ENST00000697464.1:c.*699A>C	ENSP00000513322.1:n.*699A>C
ENST00000697465.1:c.770A>C	ENSP00000513323.1:p.Asp257Ala
ENST00000697466.1:c.740A>C	ENSP00000513324.1:p.Asp247Ala
ENST00000697467.1:c.644A>C	ENSP00000513325.1:p.Asp215Ala
ENST00000697468.1:c.716A>C	ENSP00000513326.1:p.Asp239Ala
ENST00000697469.1:c.425A>C	ENSP00000513327.1:p.Asp142Ala
ENST00000697470.1:c.329A>C	ENSP00000513328.1:p.Asp110Ala
ENST00000697557.1:c.716A>C	ENSP00000513335.1:p.Asp239Ala
ENST00000521381.6:c.1733A>C MANE Select	ENSP00000428056.1:p.Asp578Ala
ENST00000320694.12:c.833A>C	ENSP00000323512.8:p.Asp278Ala
ENST00000336483.9:c.923A>C	ENSP00000338554.5:p.Asp308Ala
ENST00000517698.5:c.*703A>C	ENSP00000430424.1:n.*703A>C
ENST00000518813.5:n.2276A>C
ENST00000520550.1:n.1132A>C
ENST00000521381.5:c.1733A>C	ENSP00000428056.1:p.Asp578Ala
ENST00000521657.5:c.1733A>C	ENSP00000429277.1:p.Asp578Ala
ENST00000523872.1:c.644A>C	ENSP00000430098.1:p.Asp215Ala
NM_001242466.1:c.644A>C	NP_001229395.1:p.Asp215Ala
NM_181504.3:c.923A>C	NP_852556.2:p.Asp308Ala
NM_181523.2:c.1733A>C	NP_852664.1:p.Asp578Ala
NM_181524.1:c.833A>C	NP_852665.1:p.Asp278Ala
XM_005248542.2:c.1733A>C	XP_005248599.1:p.Asp578Ala
XM_011543493.1:c.1406A>C	XP_011541795.1:p.Asp469Ala
XM_005248542.3:c.1733A>C	XP_005248599.1:p.Asp578Ala
XM_011543493.3:c.1406A>C	XP_011541795.1:p.Asp469Ala
XM_017009585.2:c.1733A>C	XP_016865074.1:p.Asp578Ala
XM_017009586.1:c.1460A>C	XP_016865075.1:p.Asp487Ala
NM_181523.3:c.1733A>C MANE Select	NP_852664.1:p.Asp578Ala
NM_001242466.2:c.644A>C	NP_001229395.1:p.Asp215Ala
NM_181504.4:c.923A>C	NP_852556.2:p.Asp308Ala
NM_181524.2:c.833A>C	NP_852665.1:p.Asp278Ala