Canonical Allele Identifier: CA2759588720
Gene: PIK3CA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179218452_179218453insGT , CM000665.2:g.179218452_179218453insGT GRCh38
NC_000003.11:g.178936240_178936241insGT , CM000665.1:g.178936240_178936241insGT GRCh37
NC_000003.10:g.180418934_180418935insGT NCBI36
NG_012113.2:g.74930_74931insGT , LRG_310:g.74930_74931insGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000263967.4:c.1664+118_1664+119insGT MANE Select ENSP00000263967.3:n.1664+118_1664+119insGT
ENST00000462255.2:n.126+118_126+119insGT
ENST00000643187.1:c.1664+118_1664+119insGT ENSP00000493507.1:n.1664+118_1664+119insGT
ENST00000674534.1:n.1536_1537insGT
ENST00000674622.1:c.167+118_167+119insGT ENSP00000502417.1:n.167+118_167+119insGT
ENST00000675467.1:n.4471+118_4471+119insGT
ENST00000675786.1:c.*231+118_*231+119insGT ENSP00000502323.1:n.*231+118_*231+119insGT
ENST00000263967.3:c.1664+118_1664+119insGT ENSP00000263967.3:n.1664+118_1664+119insGT
NM_006218.2:c.1664+118_1664+119insGT , LRG_310t1:c.1664+118_1664+119insGT NP_006209.2:n.1664+118_1664+119insGT
XM_006713658.2:c.1664+118_1664+119insGT XP_006713721.1:n.1664+118_1664+119insGT
XM_011512894.1:c.1664+118_1664+119insGT XP_011511196.1:n.1664+118_1664+119insGT
NM_006218.3:c.1664+118_1664+119insGT NP_006209.2:n.1664+118_1664+119insGT
XM_006713658.4:c.1664+118_1664+119insGT XP_006713721.1:n.1664+118_1664+119insGT
XM_011512894.2:c.1664+118_1664+119insGT XP_011511196.1:n.1664+118_1664+119insGT
NM_006218.4:c.1664+118_1664+119insGT MANE Select NP_006209.2:n.1664+118_1664+119insGT