Canonical Allele Identifier: CA444672826

Gene: PIK3R1

Linked Data

• COSMIC: COSM1069626 ; COSM1595618 ; COSM1595619
• MyVariant Identifiers: chr5:g.67591135del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.68295307del , CM000667.2:g.68295307del	GRCh38
NC_000005.9:g.67591135del , CM000667.1:g.67591135del	GRCh37
NC_000005.8:g.67626891del	NCBI36
NG_012849.2:g.84552del

Transcript Alleles

HGVS	Amino-acid change
ENST00000320694.13:c.828del	ENSP00000323512.8:p.Arg277GlufsTer5
ENST00000336483.10:c.918del	ENSP00000338554.5:p.Arg307GlufsTer5
ENST00000517643.2:c.1728del	ENSP00000513333.1:p.Arg577GlufsTer5
ENST00000517698.6:c.*698del	ENSP00000430424.1:n.*698del
ENST00000521657.6:c.1728del	ENSP00000429277.1:p.Arg577GlufsTer5
ENST00000522084.6:c.918del	ENSP00000429766.2:p.Arg307GlufsTer5
ENST00000697457.1:c.1653del	ENSP00000513315.1:p.Arg552GlufsTer5
ENST00000697458.1:c.1728del	ENSP00000513316.1:p.Arg577GlufsTer5
ENST00000697460.1:c.1203del	ENSP00000513318.1:p.Arg402GlufsTer5
ENST00000697461.1:c.1728del	ENSP00000513319.1:p.Arg577GlufsTer5
ENST00000697462.1:c.918del	ENSP00000513320.1:p.Arg307GlufsTer5
ENST00000697463.1:n.1369del
ENST00000697464.1:c.*694del	ENSP00000513322.1:n.*694del
ENST00000697465.1:c.765del	ENSP00000513323.1:p.Arg256GlufsTer5
ENST00000697466.1:c.735del	ENSP00000513324.1:p.Arg246GlufsTer5
ENST00000697467.1:c.639del	ENSP00000513325.1:p.Arg214GlufsTer5
ENST00000697468.1:c.711del	ENSP00000513326.1:p.Arg238GlufsTer5
ENST00000697469.1:c.420del	ENSP00000513327.1:p.Arg141GlufsTer5
ENST00000697470.1:c.324del	ENSP00000513328.1:p.Arg109GlufsTer5
ENST00000697557.1:c.711del	ENSP00000513335.1:p.Arg238GlufsTer5
ENST00000521381.6:c.1728del MANE Select	ENSP00000428056.1:p.Arg577GlufsTer5
ENST00000320694.12:c.828del	ENSP00000323512.8:p.Arg277GlufsTer5
ENST00000336483.9:c.918del	ENSP00000338554.5:p.Arg307GlufsTer5
ENST00000517698.5:c.*698del	ENSP00000430424.1:n.*698del
ENST00000518813.5:n.2271del
ENST00000520550.1:n.1127del
ENST00000521381.5:c.1728del	ENSP00000428056.1:p.Arg577GlufsTer5
ENST00000521657.5:c.1728del	ENSP00000429277.1:p.Arg577GlufsTer5
ENST00000523872.1:c.639del	ENSP00000430098.1:p.Arg214GlufsTer5
NM_001242466.1:c.639del	NP_001229395.1:p.Arg214GlufsTer5
NM_181504.3:c.918del	NP_852556.2:p.Arg307GlufsTer5
NM_181523.2:c.1728del	NP_852664.1:p.Arg577GlufsTer5
NM_181524.1:c.828del	NP_852665.1:p.Arg277GlufsTer5
XM_005248542.2:c.1728del	XP_005248599.1:p.Arg577GlufsTer5
XM_011543493.1:c.1401del	XP_011541795.1:p.Arg468GlufsTer5
XM_005248542.3:c.1728del	XP_005248599.1:p.Arg577GlufsTer5
XM_011543493.3:c.1401del	XP_011541795.1:p.Arg468GlufsTer5
XM_017009585.2:c.1728del	XP_016865074.1:p.Arg577GlufsTer5
XM_017009586.1:c.1455del	XP_016865075.1:p.Arg486GlufsTer5
NM_181523.3:c.1728del MANE Select	NP_852664.1:p.Arg577GlufsTer5
NM_001242466.2:c.639del	NP_001229395.1:p.Arg214GlufsTer5
NM_181504.4:c.918del	NP_852556.2:p.Arg307GlufsTer5
NM_181524.2:c.828del	NP_852665.1:p.Arg277GlufsTer5