Canonical Allele Identifier: CA1423676457

Gene: PIK3CA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179234296C= , CM000665.2:g.179234296C=	GRCh38
NC_000003.11:g.178952084C= , CM000665.1:g.178952084C=	GRCh37
NC_000003.10:g.180434778C=	NCBI36
NG_012113.2:g.90774C= , LRG_310:g.90774C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000263967.4:c.3139C= MANE Select	ENSP00000263967.3:p.His1047=
ENST00000462255.2:n.2162C=
ENST00000643187.1:c.*219C=	ENSP00000493507.1:n.*219C=
ENST00000674534.1:n.4047C=
ENST00000674622.1:c.1560C=	ENSP00000502417.1:n.1560C=
ENST00000675467.1:n.5946C=
ENST00000675786.1:c.*1706C=	ENSP00000502323.1:n.*1706C=
ENST00000675796.1:n.3034C=
ENST00000263967.3:c.3139C=	ENSP00000263967.3:p.His1047=
NM_006218.2:c.3139C= , LRG_310t1:c.3139C=	NP_006209.2:p.His1047=
XM_006713658.2:c.3139C=	XP_006713721.1:p.His1047=
XM_011512894.1:c.3139C=	XP_011511196.1:p.His1047=
NM_006218.3:c.3139C=	NP_006209.2:p.His1047=
XM_006713658.4:c.3139C=	XP_006713721.1:p.His1047=
XM_011512894.2:c.3139C=	XP_011511196.1:p.His1047=
NM_006218.4:c.3139C= MANE Select	NP_006209.2:p.His1047=