Canonical Allele Identifier: CA2695199341

Gene: PIK3CA

Linked Data

• ClinVar Variation Id: 2672088
• ClinVar RCV Id: RCV003458278

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