Canonical Allele Identifier: CA355285682
Gene: PIK3CA HGNC NCBI

Linked Data

dbSNP Id: rs2108429697

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179234254C>A , CM000665.2:g.179234254C>A GRCh38
NC_000003.11:g.178952042C>A , CM000665.1:g.178952042C>A GRCh37
NC_000003.10:g.180434736C>A NCBI36
NG_012113.2:g.90732C>A , LRG_310:g.90732C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263967.4:c.3097C>A MANE Select ENSP00000263967.3:p.Gln1033Lys
ENST00000462255.2:n.2120C>A
ENST00000643187.1:c.*177C>A ENSP00000493507.1:n.*177C>A
ENST00000674534.1:n.4005C>A
ENST00000674622.1:c.1518C>A ENSP00000502417.1:n.1518C>A
ENST00000675467.1:n.5904C>A
ENST00000675786.1:c.*1664C>A ENSP00000502323.1:n.*1664C>A
ENST00000675796.1:n.2992C>A
ENST00000263967.3:c.3097C>A ENSP00000263967.3:p.Gln1033Lys
NM_006218.2:c.3097C>A , LRG_310t1:c.3097C>A NP_006209.2:p.Gln1033Lys
XM_006713658.2:c.3097C>A XP_006713721.1:p.Gln1033Lys
XM_011512894.1:c.3097C>A XP_011511196.1:p.Gln1033Lys
NM_006218.3:c.3097C>A NP_006209.2:p.Gln1033Lys
XM_006713658.4:c.3097C>A XP_006713721.1:p.Gln1033Lys
XM_011512894.2:c.3097C>A XP_011511196.1:p.Gln1033Lys
NM_006218.4:c.3097C>A MANE Select NP_006209.2:p.Gln1033Lys