Canonical Allele Identifier: CA2832534322
Gene: PIK3CA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179198878dup , CM000665.2:g.179198878dup GRCh38
NC_000003.11:g.178916666dup , CM000665.1:g.178916666dup GRCh37
NC_000003.10:g.180399360dup NCBI36
NG_012113.2:g.55356dup , LRG_310:g.55356dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000263967.4:c.53dup MANE Select ENSP00000263967.3:p.Arg19LysfsTer21
ENST00000643187.1:c.53dup ENSP00000493507.1:p.Arg19LysfsTer21
ENST00000675467.1:n.2860dup
ENST00000675786.1:c.53dup ENSP00000502323.1:p.Arg19LysfsTer21
ENST00000263967.3:c.53dup ENSP00000263967.3:p.Arg19LysfsTer21
ENST00000468036.1:c.53dup ENSP00000417479.1:p.Arg19LysfsTer21
ENST00000477735.1:c.53dup ENSP00000418145.1:p.Arg19LysfsTer?
NM_006218.2:c.53dup , LRG_310t1:c.53dup NP_006209.2:p.Arg19LysfsTer21
XM_006713658.2:c.53dup XP_006713721.1:p.Arg19LysfsTer21
XM_011512894.1:c.53dup XP_011511196.1:p.Arg19LysfsTer21
NM_006218.3:c.53dup NP_006209.2:p.Arg19LysfsTer21
XM_006713658.4:c.53dup XP_006713721.1:p.Arg19LysfsTer21
XM_011512894.2:c.53dup XP_011511196.1:p.Arg19LysfsTer21
NM_006218.4:c.53dup MANE Select NP_006209.2:p.Arg19LysfsTer21