Canonical Allele Identifier: CA1423674164
Gene: PIK3CA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179218321C= , CM000665.2:g.179218321C= GRCh38
NC_000003.11:g.178936109C= , CM000665.1:g.178936109C= GRCh37
NC_000003.10:g.180418803C= NCBI36
NG_012113.2:g.74799C= , LRG_310:g.74799C=

Transcript Alleles

HGVS Amino-acid change
ENST00000263967.4:c.1651C= MANE Select ENSP00000263967.3:p.Leu551=
ENST00000462255.2:n.113C=
ENST00000643187.1:c.1651C= ENSP00000493507.1:p.Leu551=
ENST00000674534.1:n.1405C=
ENST00000674622.1:c.154C= ENSP00000502417.1:p.Leu52=
ENST00000675467.1:n.4458C=
ENST00000675786.1:c.*218C= ENSP00000502323.1:n.*218C=
ENST00000263967.3:c.1651C= ENSP00000263967.3:p.Leu551=
NM_006218.2:c.1651C= , LRG_310t1:c.1651C= NP_006209.2:p.Leu551=
XM_006713658.2:c.1651C= XP_006713721.1:p.Leu551=
XM_011512894.1:c.1651C= XP_011511196.1:p.Leu551=
NM_006218.3:c.1651C= NP_006209.2:p.Leu551=
XM_006713658.4:c.1651C= XP_006713721.1:p.Leu551=
XM_011512894.2:c.1651C= XP_011511196.1:p.Leu551=
NM_006218.4:c.1651C= MANE Select NP_006209.2:p.Leu551=