Canonical Allele Identifier: CA437037924

Gene: PIK3CA

Linked Data

• MyVariant Identifiers: chr3:g.178947792A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179230004A>C , CM000665.2:g.179230004A>C	GRCh38
NC_000003.11:g.178947792A>C , CM000665.1:g.178947792A>C	GRCh37
NC_000003.10:g.180430486A>C	NCBI36
NG_012113.2:g.86482A>C , LRG_310:g.86482A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000263967.4:c.2667A>C MANE Select	ENSP00000263967.3:p.Ile889=
ENST00000462255.2:n.1690A>C
ENST00000643187.1:c.2667A>C	ENSP00000493507.1:p.Ile889=
ENST00000674534.1:n.3575A>C
ENST00000674622.1:c.1088A>C	ENSP00000502417.1:n.1088A>C
ENST00000675467.1:n.5474A>C
ENST00000675786.1:c.*1234A>C	ENSP00000502323.1:n.*1234A>C
ENST00000675796.1:n.2562A>C
ENST00000263967.3:c.2667A>C	ENSP00000263967.3:p.Ile889=
NM_006218.2:c.2667A>C , LRG_310t1:c.2667A>C	NP_006209.2:p.Ile889=
XM_006713658.2:c.2667A>C	XP_006713721.1:p.Ile889=
XM_011512894.1:c.2667A>C	XP_011511196.1:p.Ile889=
NM_006218.3:c.2667A>C	NP_006209.2:p.Ile889=
XM_006713658.4:c.2667A>C	XP_006713721.1:p.Ile889=
XM_011512894.2:c.2667A>C	XP_011511196.1:p.Ile889=
NM_006218.4:c.2667A>C MANE Select	NP_006209.2:p.Ile889=