Canonical Allele Identifier: CA645535220
Gene: PIK3CA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179199157_179199159del , CM000665.2:g.179199157_179199159del GRCh38
NC_000003.11:g.178916945_178916947del , CM000665.1:g.178916945_178916947del GRCh37
NC_000003.10:g.180399639_180399641del NCBI36
NG_012113.2:g.55635_55637del , LRG_310:g.55635_55637del

Transcript Alleles

HGVS Amino-acid Change
ENST00000263967.4:c.332_334del MANE Select ENSP00000263967.3:p.Lys111del
ENST00000643187.1:c.332_334del ENSP00000493507.1:p.Lys111del
ENST00000675467.1:n.3139_3141del
ENST00000675786.1:c.332_334del ENSP00000502323.1:p.Lys111del
ENST00000263967.3:c.332_334del ENSP00000263967.3:p.Lys111del
ENST00000468036.1:c.332_334del ENSP00000417479.1:p.Lys111del
NM_006218.2:c.332_334del , LRG_310t1:c.332_334del NP_006209.2:p.Lys111del
XM_006713658.2:c.332_334del XP_006713721.1:p.Lys111del
XM_011512894.1:c.332_334del XP_011511196.1:p.Lys111del
NM_006218.3:c.332_334del NP_006209.2:p.Lys111del
XM_006713658.4:c.332_334del XP_006713721.1:p.Lys111del
XM_011512894.2:c.332_334del XP_011511196.1:p.Lys111del
NM_006218.4:c.332_334del MANE Select NP_006209.2:p.Lys111del