Canonical Allele Identifier: CA16602700
Gene: PIK3CA HGNC NCBI

Linked Data

ClinVar Variation Id: 376247
dbSNP Id: rs121913277

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179234302G>A , CM000665.2:g.179234302G>A GRCh38
NC_000003.11:g.178952090G>A , CM000665.1:g.178952090G>A GRCh37
NC_000003.10:g.180434784G>A NCBI36
NG_012113.2:g.90780G>A , LRG_310:g.90780G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000263967.4:c.3145G>A MANE Select ENSP00000263967.3:p.Gly1049Ser
ENST00000462255.2:n.2168G>A
ENST00000643187.1:c.*225G>A ENSP00000493507.1:n.*225G>A
ENST00000674534.1:n.4053G>A
ENST00000674622.1:c.1566G>A ENSP00000502417.1:n.1566G>A
ENST00000675467.1:n.5952G>A
ENST00000675786.1:c.*1712G>A ENSP00000502323.1:n.*1712G>A
ENST00000675796.1:n.3040G>A
ENST00000263967.3:c.3145G>A ENSP00000263967.3:p.Gly1049Ser
NM_006218.2:c.3145G>A , LRG_310t1:c.3145G>A NP_006209.2:p.Gly1049Ser
XM_006713658.2:c.3145G>A XP_006713721.1:p.Gly1049Ser
XM_011512894.1:c.3145G>A XP_011511196.1:p.Gly1049Ser
NM_006218.3:c.3145G>A NP_006209.2:p.Gly1049Ser
XM_006713658.4:c.3145G>A XP_006713721.1:p.Gly1049Ser
XM_011512894.2:c.3145G>A XP_011511196.1:p.Gly1049Ser
NM_006218.4:c.3145G>A MANE Select NP_006209.2:p.Gly1049Ser