Canonical Allele Identifier: CA123342
Gene: PIK3CA HGNC NCBI

Linked Data

ClinVar Variation Id: 13659
dbSNP Id: rs121913274
CIViC: CA123342

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179218304A>C , CM000665.2:g.179218304A>C GRCh38
NC_000003.11:g.178936092A>C , CM000665.1:g.178936092A>C GRCh37
NC_000003.10:g.180418786A>C NCBI36
NG_012113.2:g.74782A>C , LRG_310:g.74782A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000263967.4:c.1634A>C MANE Select ENSP00000263967.3:p.Glu545Ala
ENST00000462255.2:n.96A>C
ENST00000643187.1:c.1634A>C ENSP00000493507.1:p.Glu545Ala
ENST00000674534.1:n.1388A>C
ENST00000674622.1:c.137A>C ENSP00000502417.1:p.Glu46Ala
ENST00000675467.1:n.4441A>C
ENST00000675786.1:c.*201A>C ENSP00000502323.1:n.*201A>C
ENST00000263967.3:c.1634A>C ENSP00000263967.3:p.Glu545Ala
NM_006218.2:c.1634A>C , LRG_310t1:c.1634A>C NP_006209.2:p.Glu545Ala
XM_006713658.2:c.1634A>C XP_006713721.1:p.Glu545Ala
XM_011512894.1:c.1634A>C XP_011511196.1:p.Glu545Ala
NM_006218.3:c.1634A>C NP_006209.2:p.Glu545Ala
XM_006713658.4:c.1634A>C XP_006713721.1:p.Glu545Ala
XM_011512894.2:c.1634A>C XP_011511196.1:p.Glu545Ala
NM_006218.4:c.1634A>C MANE Select NP_006209.2:p.Glu545Ala