Canonical Allele Identifier: CA1423676471

Gene: PIK3CA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179234355A= , CM000665.2:g.179234355A=	GRCh38
NC_000003.11:g.178952143A= , CM000665.1:g.178952143A=	GRCh37
NC_000003.10:g.180434837A=	NCBI36
NG_012113.2:g.90833A= , LRG_310:g.90833A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.3198A= MANE Select	ENSP00000263967.3:p.Ala1066=
ENST00000462255.2:n.2221A=
ENST00000643187.1:c.*278A=	ENSP00000493507.1:n.*278A=
ENST00000674534.1:n.4106A=
ENST00000674622.1:c.1619A=	ENSP00000502417.1:n.1619A=
ENST00000675467.1:n.6005A=
ENST00000675786.1:c.*1765A=	ENSP00000502323.1:n.*1765A=
ENST00000675796.1:n.3093A=
ENST00000263967.3:c.3198A=	ENSP00000263967.3:p.Ala1066=
NM_006218.2:c.3198A= , LRG_310t1:c.3198A=	NP_006209.2:p.Ala1066=
XM_006713658.2:c.3198A=	XP_006713721.1:p.Ala1066=
XM_011512894.1:c.3198A=	XP_011511196.1:p.Ala1066=
NM_006218.3:c.3198A=	NP_006209.2:p.Ala1066=
XM_006713658.4:c.3198A=	XP_006713721.1:p.Ala1066=
XM_011512894.2:c.3198A=	XP_011511196.1:p.Ala1066=
NM_006218.4:c.3198A= MANE Select	NP_006209.2:p.Ala1066=