Canonical Allele Identifier: CA2695199341
Gene: PIK3CA HGNC NCBI

Linked Data

ClinVar Variation Id: 2672088
ClinVar RCV Id: RCV003458278
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179218302_179218303delinsAA , CM000665.2:g.179218302_179218303delinsAA GRCh38
NC_000003.11:g.178936090_178936091delinsAA , CM000665.1:g.178936090_178936091delinsAA GRCh37
NC_000003.10:g.180418784_180418785delinsAA NCBI36
NG_012113.2:g.74780_74781delinsAA , LRG_310:g.74780_74781delinsAA

Transcript Alleles

HGVS Amino-acid change
ENST00000263967.4:c.1632_1633delinsAA MANE Select ENSP00000263967.3:p.Glu545Lys
ENST00000462255.2:n.94_95delinsAA
ENST00000643187.1:c.1632_1633delinsAA ENSP00000493507.1:p.Glu545Lys
ENST00000674534.1:n.1386_1387delinsAA
ENST00000674622.1:c.135_136delinsAA ENSP00000502417.1:p.Glu46Lys
ENST00000675467.1:n.4439_4440delinsAA
ENST00000675786.1:c.*199_*200delinsAA ENSP00000502323.1:n.*199_*200delinsAA
ENST00000263967.3:c.1632_1633delinsAA ENSP00000263967.3:p.Glu545Lys
NM_006218.2:c.1632_1633delinsAA , LRG_310t1:c.1632_1633delinsAA NP_006209.2:p.Glu545Lys
XM_006713658.2:c.1632_1633delinsAA XP_006713721.1:p.Glu545Lys
XM_011512894.1:c.1632_1633delinsAA XP_011511196.1:p.Glu545Lys
NM_006218.3:c.1632_1633delinsAA NP_006209.2:p.Glu545Lys
XM_006713658.4:c.1632_1633delinsAA XP_006713721.1:p.Glu545Lys
XM_011512894.2:c.1632_1633delinsAA XP_011511196.1:p.Glu545Lys
NM_006218.4:c.1632_1633delinsAA MANE Select NP_006209.2:p.Glu545Lys
Search 100 bp 5'
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