Canonical Allele Identifier: CA355266168
Gene: PIK3CA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179219623A>C , CM000665.2:g.179219623A>C GRCh38
NC_000003.11:g.178937411A>C , CM000665.1:g.178937411A>C GRCh37
NC_000003.10:g.180420105A>C NCBI36
NG_012113.2:g.76101A>C , LRG_310:g.76101A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263967.4:c.1799A>C MANE Select ENSP00000263967.3:p.Glu600Ala
ENST00000462255.2:n.261A>C
ENST00000643187.1:c.1799A>C ENSP00000493507.1:p.Glu600Ala
ENST00000674534.1:n.2707A>C
ENST00000674622.1:c.220A>C ENSP00000502417.1:n.220A>C
ENST00000675467.1:n.4606A>C
ENST00000675786.1:c.*366A>C ENSP00000502323.1:n.*366A>C
ENST00000263967.3:c.1799A>C ENSP00000263967.3:p.Glu600Ala
ENST00000462255.1:n.73A>C
NM_006218.2:c.1799A>C , LRG_310t1:c.1799A>C NP_006209.2:p.Glu600Ala
XM_006713658.2:c.1799A>C XP_006713721.1:p.Glu600Ala
XM_011512894.1:c.1799A>C XP_011511196.1:p.Glu600Ala
NM_006218.3:c.1799A>C NP_006209.2:p.Glu600Ala
XM_006713658.4:c.1799A>C XP_006713721.1:p.Glu600Ala
XM_011512894.2:c.1799A>C XP_011511196.1:p.Glu600Ala
NM_006218.4:c.1799A>C MANE Select NP_006209.2:p.Glu600Ala