Canonical Allele Identifier: CA1423674133

Gene: PIK3CA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179218221A= , CM000665.2:g.179218221A=	GRCh38
NC_000003.11:g.178936009A= , CM000665.1:g.178936009A=	GRCh37
NC_000003.10:g.180418703A=	NCBI36
NG_012113.2:g.74699A= , LRG_310:g.74699A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.1551A= MANE Select	ENSP00000263967.3:p.Leu517=
ENST00000462255.2:n.13A=
ENST00000643187.1:c.1551A=	ENSP00000493507.1:p.Leu517=
ENST00000674534.1:n.1305A=
ENST00000674622.1:c.54A=	ENSP00000502417.1:p.Leu18=
ENST00000675467.1:n.4358A=
ENST00000675786.1:c.*118A=	ENSP00000502323.1:n.*118A=
ENST00000263967.3:c.1551A=	ENSP00000263967.3:p.Leu517=
NM_006218.2:c.1551A= , LRG_310t1:c.1551A=	NP_006209.2:p.Leu517=
XM_006713658.2:c.1551A=	XP_006713721.1:p.Leu517=
XM_011512894.1:c.1551A=	XP_011511196.1:p.Leu517=
NM_006218.3:c.1551A=	NP_006209.2:p.Leu517=
XM_006713658.4:c.1551A=	XP_006713721.1:p.Leu517=
XM_011512894.2:c.1551A=	XP_011511196.1:p.Leu517=
NM_006218.4:c.1551A= MANE Select	NP_006209.2:p.Leu517=