Canonical Allele Identifier: CA355265032
Gene: PIK3CA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179218292C>A , CM000665.2:g.179218292C>A GRCh38
NC_000003.11:g.178936080C>A , CM000665.1:g.178936080C>A GRCh37
NC_000003.10:g.180418774C>A NCBI36
NG_012113.2:g.74770C>A , LRG_310:g.74770C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263967.4:c.1622C>A MANE Select ENSP00000263967.3:p.Ser541Tyr
ENST00000462255.2:n.84C>A
ENST00000643187.1:c.1622C>A ENSP00000493507.1:p.Ser541Tyr
ENST00000674534.1:n.1376C>A
ENST00000674622.1:c.125C>A ENSP00000502417.1:p.Ser42Tyr
ENST00000675467.1:n.4429C>A
ENST00000675786.1:c.*189C>A ENSP00000502323.1:n.*189C>A
ENST00000263967.3:c.1622C>A ENSP00000263967.3:p.Ser541Tyr
NM_006218.2:c.1622C>A , LRG_310t1:c.1622C>A NP_006209.2:p.Ser541Tyr
XM_006713658.2:c.1622C>A XP_006713721.1:p.Ser541Tyr
XM_011512894.1:c.1622C>A XP_011511196.1:p.Ser541Tyr
NM_006218.3:c.1622C>A NP_006209.2:p.Ser541Tyr
XM_006713658.4:c.1622C>A XP_006713721.1:p.Ser541Tyr
XM_011512894.2:c.1622C>A XP_011511196.1:p.Ser541Tyr
NM_006218.4:c.1622C>A MANE Select NP_006209.2:p.Ser541Tyr