Canonical Allele Identifier: CA355285482
Gene: PIK3CA HGNC NCBI

Linked Data

dbSNP Id: rs2108429549

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179234225G>A , CM000665.2:g.179234225G>A GRCh38
NC_000003.11:g.178952013G>A , CM000665.1:g.178952013G>A GRCh37
NC_000003.10:g.180434707G>A NCBI36
NG_012113.2:g.90703G>A , LRG_310:g.90703G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000263967.4:c.3068G>A MANE Select ENSP00000263967.3:p.Arg1023Gln
ENST00000462255.2:n.2091G>A
ENST00000643187.1:c.*148G>A ENSP00000493507.1:n.*148G>A
ENST00000674534.1:n.3976G>A
ENST00000674622.1:c.1489G>A ENSP00000502417.1:n.1489G>A
ENST00000675467.1:n.5875G>A
ENST00000675786.1:c.*1635G>A ENSP00000502323.1:n.*1635G>A
ENST00000675796.1:n.2963G>A
ENST00000263967.3:c.3068G>A ENSP00000263967.3:p.Arg1023Gln
NM_006218.2:c.3068G>A , LRG_310t1:c.3068G>A NP_006209.2:p.Arg1023Gln
XM_006713658.2:c.3068G>A XP_006713721.1:p.Arg1023Gln
XM_011512894.1:c.3068G>A XP_011511196.1:p.Arg1023Gln
NM_006218.3:c.3068G>A NP_006209.2:p.Arg1023Gln
XM_006713658.4:c.3068G>A XP_006713721.1:p.Arg1023Gln
XM_011512894.2:c.3068G>A XP_011511196.1:p.Arg1023Gln
NM_006218.4:c.3068G>A MANE Select NP_006209.2:p.Arg1023Gln