Canonical Allele Identifier: CA355264450
Gene: PIK3CA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179218210A>T , CM000665.2:g.179218210A>T GRCh38
NC_000003.11:g.178935998A>T , CM000665.1:g.178935998A>T GRCh37
NC_000003.10:g.180418692A>T NCBI36
NG_012113.2:g.74688A>T , LRG_310:g.74688A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000263967.4:c.1540A>T MANE Select ENSP00000263967.3:p.Ser514Cys
ENST00000462255.2:n.2A>T
ENST00000643187.1:c.1540A>T ENSP00000493507.1:p.Ser514Cys
ENST00000674534.1:n.1294A>T
ENST00000674622.1:c.43A>T ENSP00000502417.1:p.Ser15Cys
ENST00000675467.1:n.4347A>T
ENST00000675786.1:c.*107A>T ENSP00000502323.1:n.*107A>T
ENST00000263967.3:c.1540A>T ENSP00000263967.3:p.Ser514Cys
NM_006218.2:c.1540A>T , LRG_310t1:c.1540A>T NP_006209.2:p.Ser514Cys
XM_006713658.2:c.1540A>T XP_006713721.1:p.Ser514Cys
XM_011512894.1:c.1540A>T XP_011511196.1:p.Ser514Cys
NM_006218.3:c.1540A>T NP_006209.2:p.Ser514Cys
XM_006713658.4:c.1540A>T XP_006713721.1:p.Ser514Cys
XM_011512894.2:c.1540A>T XP_011511196.1:p.Ser514Cys
NM_006218.4:c.1540A>T MANE Select NP_006209.2:p.Ser514Cys