Canonical Allele Identifier: CA891841816
Gene: PIK3CA HGNC NCBI

Linked Data

dbSNP Id: rs2108386355

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179199152_179199160del , CM000665.2:g.179199152_179199160del GRCh38
NC_000003.11:g.178916940_178916948del , CM000665.1:g.178916940_178916948del GRCh37
NC_000003.10:g.180399634_180399642del NCBI36
NG_012113.2:g.55630_55638del , LRG_310:g.55630_55638del

Transcript Alleles

HGVS Amino-acid Change
ENST00000263967.4:c.327_335del MANE Select ENSP00000263967.3:p.Glu109_Ile112delinsAsp
ENST00000643187.1:c.327_335del ENSP00000493507.1:p.Glu109_Ile112delinsAsp
ENST00000675467.1:n.3134_3142del
ENST00000675786.1:c.327_335del ENSP00000502323.1:p.Glu109_Ile112delinsAsp
ENST00000263967.3:c.327_335del ENSP00000263967.3:p.Glu109_Ile112delinsAsp
ENST00000468036.1:c.327_335del ENSP00000417479.1:p.Glu109_Ile112delinsAsp
NM_006218.2:c.327_335del , LRG_310t1:c.327_335del NP_006209.2:p.Glu109_Ile112delinsAsp
XM_006713658.2:c.327_335del XP_006713721.1:p.Glu109_Ile112delinsAsp
XM_011512894.1:c.327_335del XP_011511196.1:p.Glu109_Ile112delinsAsp
NM_006218.3:c.327_335del NP_006209.2:p.Glu109_Ile112delinsAsp
XM_006713658.4:c.327_335del XP_006713721.1:p.Glu109_Ile112delinsAsp
XM_011512894.2:c.327_335del XP_011511196.1:p.Glu109_Ile112delinsAsp
NM_006218.4:c.327_335del MANE Select NP_006209.2:p.Glu109_Ile112delinsAsp