Canonical Allele Identifier: CA2668619658
Gene: PIK3CA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179198724del , CM000665.2:g.179198724del GRCh38
NC_000003.11:g.178916512del , CM000665.1:g.178916512del GRCh37
NC_000003.10:g.180399206del NCBI36
NG_012113.2:g.55202del , LRG_310:g.55202del

Transcript Alleles

HGVS Amino-acid Change
ENST00000263967.4:c.-76-26del MANE Select ENSP00000263967.3:n.-76-26del
ENST00000643187.1:c.-76-26del ENSP00000493507.1:n.-76-26del
ENST00000675467.1:n.2706del
ENST00000675786.1:c.-76-26del ENSP00000502323.1:n.-76-26del
ENST00000263967.3:c.-76-26del ENSP00000263967.3:n.-76-26del
ENST00000468036.1:c.-76-26del ENSP00000417479.1:n.-76-26del
ENST00000477735.1:c.-76-26del ENSP00000418145.1:n.-76-26del
NM_006218.2:c.-76-26del , LRG_310t1:c.-76-26del NP_006209.2:n.-76-26del
XM_006713658.2:c.-76-26del XP_006713721.1:n.-76-26del
XM_011512894.1:c.-76-26del XP_011511196.1:n.-76-26del
NM_006218.3:c.-76-26del NP_006209.2:n.-76-26del
XM_006713658.4:c.-76-26del XP_006713721.1:n.-76-26del
XM_011512894.2:c.-76-26del XP_011511196.1:n.-76-26del
NM_006218.4:c.-76-26del MANE Select NP_006209.2:n.-76-26del