Canonical Allele Identifier: CA2577963160
Gene: PIK3CA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179219643_179219644del , CM000665.2:g.179219643_179219644del GRCh38
NC_000003.11:g.178937431_178937432del , CM000665.1:g.178937431_178937432del GRCh37
NC_000003.10:g.180420125_180420126del NCBI36
NG_012113.2:g.76121_76122del , LRG_310:g.76121_76122del

Transcript Alleles

HGVS Amino-acid Change
ENST00000263967.4:c.1819_1820del MANE Select ENSP00000263967.3:p.Pro607ArgfsTer19
ENST00000462255.2:n.281_282del
ENST00000643187.1:c.1819_1820del ENSP00000493507.1:p.Pro607ArgfsTer19
ENST00000674534.1:n.2727_2728del
ENST00000674622.1:c.240_241del ENSP00000502417.1:n.240_241del
ENST00000675467.1:n.4626_4627del
ENST00000675786.1:c.*386_*387del ENSP00000502323.1:n.*386_*387del
ENST00000263967.3:c.1819_1820del ENSP00000263967.3:p.Pro607ArgfsTer19
ENST00000462255.1:n.93_94del
NM_006218.2:c.1819_1820del , LRG_310t1:c.1819_1820del NP_006209.2:p.Pro607ArgfsTer19
XM_006713658.2:c.1819_1820del XP_006713721.1:p.Pro607ArgfsTer19
XM_011512894.1:c.1819_1820del XP_011511196.1:p.Pro607ArgfsTer19
NM_006218.3:c.1819_1820del NP_006209.2:p.Pro607ArgfsTer19
XM_006713658.4:c.1819_1820del XP_006713721.1:p.Pro607ArgfsTer19
XM_011512894.2:c.1819_1820del XP_011511196.1:p.Pro607ArgfsTer19
NM_006218.4:c.1819_1820del MANE Select NP_006209.2:p.Pro607ArgfsTer19