Canonical Allele Identifier: CA645517360

Gene: PIK3CA

Linked Data

• COSMIC: COSM142977 ; COSM142978

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179234237_179234238delinsTT , CM000665.2:g.179234237_179234238delinsTT	GRCh38
NC_000003.11:g.178952025_178952026delinsTT , CM000665.1:g.178952025_178952026delinsTT	GRCh37
NC_000003.10:g.180434719_180434720delinsTT	NCBI36
NG_012113.2:g.90715_90716delinsTT , LRG_310:g.90715_90716delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.3080_3081delinsTT MANE Select	ENSP00000263967.3:p.Ala1027Val
ENST00000462255.2:n.2103_2104delinsTT
ENST00000643187.1:c.*160_*161delinsTT	ENSP00000493507.1:n.*160_*161delinsTT
ENST00000674534.1:n.3988_3989delinsTT
ENST00000674622.1:c.1501_1502delinsTT	ENSP00000502417.1:n.1501_1502delinsTT
ENST00000675467.1:n.5887_5888delinsTT
ENST00000675786.1:c.*1647_*1648delinsTT	ENSP00000502323.1:n.*1647_*1648delinsTT
ENST00000675796.1:n.2975_2976delinsTT
ENST00000263967.3:c.3080_3081delinsTT	ENSP00000263967.3:p.Ala1027Val
NM_006218.2:c.3080_3081delinsTT , LRG_310t1:c.3080_3081delinsTT	NP_006209.2:p.Ala1027Val
XM_006713658.2:c.3080_3081delinsTT	XP_006713721.1:p.Ala1027Val
XM_011512894.1:c.3080_3081delinsTT	XP_011511196.1:p.Ala1027Val
NM_006218.3:c.3080_3081delinsTT	NP_006209.2:p.Ala1027Val
XM_006713658.4:c.3080_3081delinsTT	XP_006713721.1:p.Ala1027Val
XM_011512894.2:c.3080_3081delinsTT	XP_011511196.1:p.Ala1027Val
NM_006218.4:c.3080_3081delinsTT MANE Select	NP_006209.2:p.Ala1027Val