Canonical Allele Identifier: CA1423676458

Gene: PIK3CA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179234297A= , CM000665.2:g.179234297A=	GRCh38
NC_000003.11:g.178952085A= , CM000665.1:g.178952085A=	GRCh37
NC_000003.10:g.180434779A=	NCBI36
NG_012113.2:g.90775A= , LRG_310:g.90775A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.3140A= MANE Select	ENSP00000263967.3:p.His1047=
ENST00000462255.2:n.2163A=
ENST00000643187.1:c.*220A=	ENSP00000493507.1:n.*220A=
ENST00000674534.1:n.4048A=
ENST00000674622.1:c.1561A=	ENSP00000502417.1:n.1561A=
ENST00000675467.1:n.5947A=
ENST00000675786.1:c.*1707A=	ENSP00000502323.1:n.*1707A=
ENST00000675796.1:n.3035A=
ENST00000263967.3:c.3140A=	ENSP00000263967.3:p.His1047=
NM_006218.2:c.3140A= , LRG_310t1:c.3140A=	NP_006209.2:p.His1047=
XM_006713658.2:c.3140A=	XP_006713721.1:p.His1047=
XM_011512894.1:c.3140A=	XP_011511196.1:p.His1047=
NM_006218.3:c.3140A=	NP_006209.2:p.His1047=
XM_006713658.4:c.3140A=	XP_006713721.1:p.His1047=
XM_011512894.2:c.3140A=	XP_011511196.1:p.His1047=
NM_006218.4:c.3140A= MANE Select	NP_006209.2:p.His1047=