Canonical Allele Identifier: CA645535227

Gene: PIK3CA

Linked Data

• COSMIC: COSM5547414 ; COSM5547415

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179199166_179199168del , CM000665.2:g.179199166_179199168del	GRCh38
NC_000003.11:g.178916954_178916956del , CM000665.1:g.178916954_178916956del	GRCh37
NC_000003.10:g.180399648_180399650del	NCBI36
NG_012113.2:g.55644_55646del , LRG_310:g.55644_55646del

Transcript Alleles

HGVS	Amino-acid change
ENST00000263967.4:c.341_343del MANE Select	ENSP00000263967.3:p.Asn114del
ENST00000643187.1:c.341_343del	ENSP00000493507.1:p.Asn114del
ENST00000675467.1:n.3148_3150del
ENST00000675786.1:c.341_343del	ENSP00000502323.1:p.Asn114del
ENST00000263967.3:c.341_343del	ENSP00000263967.3:p.Asn114del
ENST00000468036.1:c.341_343del	ENSP00000417479.1:p.Asn114del
NM_006218.2:c.341_343del , LRG_310t1:c.341_343del	NP_006209.2:p.Asn114del
XM_006713658.2:c.341_343del	XP_006713721.1:p.Asn114del
XM_011512894.1:c.341_343del	XP_011511196.1:p.Asn114del
NM_006218.3:c.341_343del	NP_006209.2:p.Asn114del
XM_006713658.4:c.341_343del	XP_006713721.1:p.Asn114del
XM_011512894.2:c.341_343del	XP_011511196.1:p.Asn114del
NM_006218.4:c.341_343del MANE Select	NP_006209.2:p.Asn114del