Canonical Allele Identifier: CA645556598
Gene: PIK3R1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.68295280_68295290del , CM000667.2:g.68295280_68295290del GRCh38
NC_000005.9:g.67591108_67591118del , CM000667.1:g.67591108_67591118del GRCh37
NC_000005.8:g.67626864_67626874del NCBI36
NG_012849.2:g.84525_84535del

Transcript Alleles

HGVS Amino-acid Change
ENST00000320694.13:c.801_811del ENSP00000323512.8:p.Lys267AsnfsTer?
ENST00000336483.10:c.891_901del ENSP00000338554.5:p.Lys297AsnfsTer?
ENST00000517643.2:c.1701_1711del ENSP00000513333.1:p.Lys567AsnfsTer?
ENST00000517698.6:c.*671_*681del ENSP00000430424.1:n.*671_*681del
ENST00000521657.6:c.1701_1711del ENSP00000429277.1:p.Lys567AsnfsTer?
ENST00000522084.6:c.891_901del ENSP00000429766.2:p.Lys297AsnfsTer?
ENST00000697457.1:c.1626_1636del ENSP00000513315.1:p.Lys542AsnfsTer?
ENST00000697458.1:c.1701_1711del ENSP00000513316.1:p.Lys567AsnfsTer?
ENST00000697460.1:c.1176_1186del ENSP00000513318.1:p.Lys392AsnfsTer?
ENST00000697461.1:c.1701_1711del ENSP00000513319.1:p.Lys567AsnfsTer?
ENST00000697462.1:c.891_901del ENSP00000513320.1:p.Lys297AsnfsTer?
ENST00000697463.1:n.1342_1352del
ENST00000697464.1:c.*667_*677del ENSP00000513322.1:n.*667_*677del
ENST00000697465.1:c.738_748del ENSP00000513323.1:p.Lys246AsnfsTer?
ENST00000697466.1:c.708_718del ENSP00000513324.1:p.Lys236AsnfsTer?
ENST00000697467.1:c.612_622del ENSP00000513325.1:p.Lys204AsnfsTer?
ENST00000697468.1:c.684_694del ENSP00000513326.1:p.Lys228AsnfsTer?
ENST00000697469.1:c.393_403del ENSP00000513327.1:p.Lys131AsnfsTer?
ENST00000697470.1:c.297_307del ENSP00000513328.1:p.Lys99AsnfsTer?
ENST00000697557.1:c.684_694del ENSP00000513335.1:p.Lys228AsnfsTer?
ENST00000521381.6:c.1701_1711del MANE Select ENSP00000428056.1:p.Lys567AsnfsTer?
ENST00000320694.12:c.801_811del ENSP00000323512.8:p.Lys267AsnfsTer?
ENST00000336483.9:c.891_901del ENSP00000338554.5:p.Lys297AsnfsTer?
ENST00000517698.5:c.*671_*681del ENSP00000430424.1:n.*671_*681del
ENST00000518813.5:n.2244_2254del
ENST00000520550.1:n.1100_1110del
ENST00000521381.5:c.1701_1711del ENSP00000428056.1:p.Lys567AsnfsTer?
ENST00000521657.5:c.1701_1711del ENSP00000429277.1:p.Lys567AsnfsTer?
ENST00000523872.1:c.612_622del ENSP00000430098.1:p.Lys204AsnfsTer?
NM_001242466.1:c.612_622del NP_001229395.1:p.Lys204AsnfsTer?
NM_181504.3:c.891_901del NP_852556.2:p.Lys297AsnfsTer?
NM_181523.2:c.1701_1711del NP_852664.1:p.Lys567AsnfsTer?
NM_181524.1:c.801_811del NP_852665.1:p.Lys267AsnfsTer?
XM_005248542.2:c.1701_1711del XP_005248599.1:p.Lys567AsnfsTer?
XM_011543493.1:c.1374_1384del XP_011541795.1:p.Lys458AsnfsTer?
XM_005248542.3:c.1701_1711del XP_005248599.1:p.Lys567AsnfsTer?
XM_011543493.3:c.1374_1384del XP_011541795.1:p.Lys458AsnfsTer?
XM_017009585.2:c.1701_1711del XP_016865074.1:p.Lys567AsnfsTer?
XM_017009586.1:c.1428_1438del XP_016865075.1:p.Lys476AsnfsTer?
NM_181523.3:c.1701_1711del MANE Select NP_852664.1:p.Lys567AsnfsTer?
NM_001242466.2:c.612_622del NP_001229395.1:p.Lys204AsnfsTer?
NM_181504.4:c.891_901del NP_852556.2:p.Lys297AsnfsTer?
NM_181524.2:c.801_811del NP_852665.1:p.Lys267AsnfsTer?