Canonical Allele Identifier: CA1423674666
Gene: PIK3CA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179219586A= , CM000665.2:g.179219586A= GRCh38
NC_000003.11:g.178937374A= , CM000665.1:g.178937374A= GRCh37
NC_000003.10:g.180420068A= NCBI36
NG_012113.2:g.76064A= , LRG_310:g.76064A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263967.4:c.1762A= MANE Select ENSP00000263967.3:p.Lys588=
ENST00000462255.2:n.224A=
ENST00000643187.1:c.1762A= ENSP00000493507.1:p.Lys588=
ENST00000674534.1:n.2670A=
ENST00000674622.1:c.183A= ENSP00000502417.1:p.Ter61=
ENST00000675467.1:n.4569A=
ENST00000675786.1:c.*329A= ENSP00000502323.1:n.*329A=
ENST00000263967.3:c.1762A= ENSP00000263967.3:p.Lys588=
ENST00000462255.1:n.36A=
NM_006218.2:c.1762A= , LRG_310t1:c.1762A= NP_006209.2:p.Lys588=
XM_006713658.2:c.1762A= XP_006713721.1:p.Lys588=
XM_011512894.1:c.1762A= XP_011511196.1:p.Lys588=
NM_006218.3:c.1762A= NP_006209.2:p.Lys588=
XM_006713658.4:c.1762A= XP_006713721.1:p.Lys588=
XM_011512894.2:c.1762A= XP_011511196.1:p.Lys588=
NM_006218.4:c.1762A= MANE Select NP_006209.2:p.Lys588=