Canonical Allele Identifier: CA1423674179

Gene: PIK3CA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179218355T= , CM000665.2:g.179218355T=	GRCh38
NC_000003.11:g.178936143T= , CM000665.1:g.178936143T=	GRCh37
NC_000003.10:g.180418837T=	NCBI36
NG_012113.2:g.74833T= , LRG_310:g.74833T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.1664+21T= MANE Select	ENSP00000263967.3:n.1664+21T=
ENST00000462255.2:n.126+21T=
ENST00000643187.1:c.1664+21T=	ENSP00000493507.1:n.1664+21T=
ENST00000674534.1:n.1439T=
ENST00000674622.1:c.167+21T=	ENSP00000502417.1:n.167+21T=
ENST00000675467.1:n.4471+21T=
ENST00000675786.1:c.*231+21T=	ENSP00000502323.1:n.*231+21T=
ENST00000263967.3:c.1664+21T=	ENSP00000263967.3:n.1664+21T=
NM_006218.2:c.1664+21T= , LRG_310t1:c.1664+21T=	NP_006209.2:n.1664+21T=
XM_006713658.2:c.1664+21T=	XP_006713721.1:n.1664+21T=
XM_011512894.1:c.1664+21T=	XP_011511196.1:n.1664+21T=
NM_006218.3:c.1664+21T=	NP_006209.2:n.1664+21T=
XM_006713658.4:c.1664+21T=	XP_006713721.1:n.1664+21T=
XM_011512894.2:c.1664+21T=	XP_011511196.1:n.1664+21T=
NM_006218.4:c.1664+21T= MANE Select	NP_006209.2:n.1664+21T=