Canonical Allele Identifier: CA2704641979
Gene: PIK3CA HGNC NCBI

Linked Data

dbSNP Id: rs2108408589

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179218368_179218373dup , CM000665.2:g.179218368_179218373dup GRCh38
NC_000003.11:g.178936156_178936161dup , CM000665.1:g.178936156_178936161dup GRCh37
NC_000003.10:g.180418850_180418855dup NCBI36
NG_012113.2:g.74846_74851dup , LRG_310:g.74846_74851dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000263967.4:c.1664+34_1664+39dup MANE Select ENSP00000263967.3:n.1664+34_1664+39dup
ENST00000462255.2:n.126+34_126+39dup
ENST00000643187.1:c.1664+34_1664+39dup ENSP00000493507.1:n.1664+34_1664+39dup
ENST00000674534.1:n.1452_1457dup
ENST00000674622.1:c.167+34_167+39dup ENSP00000502417.1:n.167+34_167+39dup
ENST00000675467.1:n.4471+34_4471+39dup
ENST00000675786.1:c.*231+34_*231+39dup ENSP00000502323.1:n.*231+34_*231+39dup
ENST00000263967.3:c.1664+34_1664+39dup ENSP00000263967.3:n.1664+34_1664+39dup
NM_006218.2:c.1664+34_1664+39dup , LRG_310t1:c.1664+34_1664+39dup NP_006209.2:n.1664+34_1664+39dup
XM_006713658.2:c.1664+34_1664+39dup XP_006713721.1:n.1664+34_1664+39dup
XM_011512894.1:c.1664+34_1664+39dup XP_011511196.1:n.1664+34_1664+39dup
NM_006218.3:c.1664+34_1664+39dup NP_006209.2:n.1664+34_1664+39dup
XM_006713658.4:c.1664+34_1664+39dup XP_006713721.1:n.1664+34_1664+39dup
XM_011512894.2:c.1664+34_1664+39dup XP_011511196.1:n.1664+34_1664+39dup
NM_006218.4:c.1664+34_1664+39dup MANE Select NP_006209.2:n.1664+34_1664+39dup