Canonical Allele Identifier: CA355264718
Gene: PIK3CA HGNC NCBI

Linked Data

dbSNP Id: rs2108408052

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179218243G>C , CM000665.2:g.179218243G>C GRCh38
NC_000003.11:g.178936031G>C , CM000665.1:g.178936031G>C GRCh37
NC_000003.10:g.180418725G>C NCBI36
NG_012113.2:g.74721G>C , LRG_310:g.74721G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263967.4:c.1573G>C MANE Select ENSP00000263967.3:p.Glu525Gln
ENST00000462255.2:n.35G>C
ENST00000643187.1:c.1573G>C ENSP00000493507.1:p.Glu525Gln
ENST00000674534.1:n.1327G>C
ENST00000674622.1:c.76G>C ENSP00000502417.1:p.Glu26Gln
ENST00000675467.1:n.4380G>C
ENST00000675786.1:c.*140G>C ENSP00000502323.1:n.*140G>C
ENST00000263967.3:c.1573G>C ENSP00000263967.3:p.Glu525Gln
NM_006218.2:c.1573G>C , LRG_310t1:c.1573G>C NP_006209.2:p.Glu525Gln
XM_006713658.2:c.1573G>C XP_006713721.1:p.Glu525Gln
XM_011512894.1:c.1573G>C XP_011511196.1:p.Glu525Gln
NM_006218.3:c.1573G>C NP_006209.2:p.Glu525Gln
XM_006713658.4:c.1573G>C XP_006713721.1:p.Glu525Gln
XM_011512894.2:c.1573G>C XP_011511196.1:p.Glu525Gln
NM_006218.4:c.1573G>C MANE Select NP_006209.2:p.Glu525Gln