Canonical Allele Identifier: CA2668622481
Gene: PIK3CA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179218363_179218364insTTTT , CM000665.2:g.179218363_179218364insTTTT GRCh38
NC_000003.11:g.178936151_178936152insTTTT , CM000665.1:g.178936151_178936152insTTTT GRCh37
NC_000003.10:g.180418845_180418846insTTTT NCBI36
NG_012113.2:g.74841_74842insTTTT , LRG_310:g.74841_74842insTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000263967.4:c.1664+29_1664+30insTTTT MANE Select ENSP00000263967.3:n.1664+29_1664+30insTTTT
ENST00000462255.2:n.126+29_126+30insTTTT
ENST00000643187.1:c.1664+29_1664+30insTTTT ENSP00000493507.1:n.1664+29_1664+30insTTTT
ENST00000674534.1:n.1447_1448insTTTT
ENST00000674622.1:c.167+29_167+30insTTTT ENSP00000502417.1:n.167+29_167+30insTTTT
ENST00000675467.1:n.4471+29_4471+30insTTTT
ENST00000675786.1:c.*231+29_*231+30insTTTT ENSP00000502323.1:n.*231+29_*231+30insTTTT
ENST00000263967.3:c.1664+29_1664+30insTTTT ENSP00000263967.3:n.1664+29_1664+30insTTTT
NM_006218.2:c.1664+29_1664+30insTTTT , LRG_310t1:c.1664+29_1664+30insTTTT NP_006209.2:n.1664+29_1664+30insTTTT
XM_006713658.2:c.1664+29_1664+30insTTTT XP_006713721.1:n.1664+29_1664+30insTTTT
XM_011512894.1:c.1664+29_1664+30insTTTT XP_011511196.1:n.1664+29_1664+30insTTTT
NM_006218.3:c.1664+29_1664+30insTTTT NP_006209.2:n.1664+29_1664+30insTTTT
XM_006713658.4:c.1664+29_1664+30insTTTT XP_006713721.1:n.1664+29_1664+30insTTTT
XM_011512894.2:c.1664+29_1664+30insTTTT XP_011511196.1:n.1664+29_1664+30insTTTT
NM_006218.4:c.1664+29_1664+30insTTTT MANE Select NP_006209.2:n.1664+29_1664+30insTTTT