Canonical Allele Identifier: CA1423674166
Gene: PIK3CA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179218327_179218329delinsAGT , CM000665.2:g.179218327_179218329delinsAGT GRCh38
NC_000003.11:g.178936115_178936117delinsAGT , CM000665.1:g.178936115_178936117delinsAGT GRCh37
NC_000003.10:g.180418809_180418811delinsAGT NCBI36
NG_012113.2:g.74805_74807delinsAGT , LRG_310:g.74805_74807delinsAGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000263967.4:c.1657_1659delinsAGT MANE Select ENSP00000263967.3:p.Ser553=
ENST00000462255.2:n.119_121delinsAGT
ENST00000643187.1:c.1657_1659delinsAGT ENSP00000493507.1:p.Ser553=
ENST00000674534.1:n.1411_1413delinsAGT
ENST00000674622.1:c.160_162delinsAGT ENSP00000502417.1:p.Ser54=
ENST00000675467.1:n.4464_4466delinsAGT
ENST00000675786.1:c.*224_*226delinsAGT ENSP00000502323.1:n.*224_*226delinsAGT
ENST00000263967.3:c.1657_1659delinsAGT ENSP00000263967.3:p.Ser553=
NM_006218.2:c.1657_1659delinsAGT , LRG_310t1:c.1657_1659delinsAGT NP_006209.2:p.Ser553=
XM_006713658.2:c.1657_1659delinsAGT XP_006713721.1:p.Ser553=
XM_011512894.1:c.1657_1659delinsAGT XP_011511196.1:p.Ser553=
NM_006218.3:c.1657_1659delinsAGT NP_006209.2:p.Ser553=
XM_006713658.4:c.1657_1659delinsAGT XP_006713721.1:p.Ser553=
XM_011512894.2:c.1657_1659delinsAGT XP_011511196.1:p.Ser553=
NM_006218.4:c.1657_1659delinsAGT MANE Select NP_006209.2:p.Ser553=