Canonical Allele Identifier: CA1423674186

Gene: PIK3CA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179218382A= , CM000665.2:g.179218382A=	GRCh38
NC_000003.11:g.178936170A= , CM000665.1:g.178936170A=	GRCh37
NC_000003.10:g.180418864A=	NCBI36
NG_012113.2:g.74860A= , LRG_310:g.74860A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.1664+48A= MANE Select	ENSP00000263967.3:n.1664+48A=
ENST00000462255.2:n.126+48A=
ENST00000643187.1:c.1664+48A=	ENSP00000493507.1:n.1664+48A=
ENST00000674534.1:n.1466A=
ENST00000674622.1:c.167+48A=	ENSP00000502417.1:n.167+48A=
ENST00000675467.1:n.4471+48A=
ENST00000675786.1:c.*231+48A=	ENSP00000502323.1:n.*231+48A=
ENST00000263967.3:c.1664+48A=	ENSP00000263967.3:n.1664+48A=
NM_006218.2:c.1664+48A= , LRG_310t1:c.1664+48A=	NP_006209.2:n.1664+48A=
XM_006713658.2:c.1664+48A=	XP_006713721.1:n.1664+48A=
XM_011512894.1:c.1664+48A=	XP_011511196.1:n.1664+48A=
NM_006218.3:c.1664+48A=	NP_006209.2:n.1664+48A=
XM_006713658.4:c.1664+48A=	XP_006713721.1:n.1664+48A=
XM_011512894.2:c.1664+48A=	XP_011511196.1:n.1664+48A=
NM_006218.4:c.1664+48A= MANE Select	NP_006209.2:n.1664+48A=