Canonical Allele Identifier: CA2759588673
Gene: PIK3CA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179214669C>A , CM000665.2:g.179214669C>A GRCh38
NC_000003.11:g.178932457C>A , CM000665.1:g.178932457C>A GRCh37
NC_000003.10:g.180415151C>A NCBI36
NG_012113.2:g.71147C>A , LRG_310:g.71147C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263967.4:c.1540-3541C>A MANE Select ENSP00000263967.3:n.1540-3541C>A
ENST00000643187.1:c.1540-3541C>A ENSP00000493507.1:n.1540-3541C>A
ENST00000674534.1:n.1294-3541C>A
ENST00000674622.1:c.43-3541C>A ENSP00000502417.1:n.43-3541C>A
ENST00000675467.1:n.4347-3541C>A
ENST00000675786.1:c.*107-3541C>A ENSP00000502323.1:n.*107-3541C>A
ENST00000263967.3:c.1540-3541C>A ENSP00000263967.3:n.1540-3541C>A
NM_006218.2:c.1540-3541C>A , LRG_310t1:c.1540-3541C>A NP_006209.2:n.1540-3541C>A
XM_006713658.2:c.1540-3541C>A XP_006713721.1:n.1540-3541C>A
XM_011512894.1:c.1540-3541C>A XP_011511196.1:n.1540-3541C>A
NM_006218.3:c.1540-3541C>A NP_006209.2:n.1540-3541C>A
XM_006713658.4:c.1540-3541C>A XP_006713721.1:n.1540-3541C>A
XM_011512894.2:c.1540-3541C>A XP_011511196.1:n.1540-3541C>A
NM_006218.4:c.1540-3541C>A MANE Select NP_006209.2:n.1540-3541C>A