Canonical Allele Identifier: CA355268811

Gene: PIK3CA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179221018G>C , CM000665.2:g.179221018G>C	GRCh38
NC_000003.11:g.178938806G>C , CM000665.1:g.178938806G>C	GRCh37
NC_000003.10:g.180421500G>C	NCBI36
NG_012113.2:g.77496G>C , LRG_310:g.77496G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_006218.4:c.2048G>C MANE Select	NP_006209.2:p.Arg683Thr
ENST00000263967.4:c.2048G>C MANE Select	ENSP00000263967.3:p.Arg683Thr
NM_006218.2:c.2048G>C , LRG_310t1:c.2048G>C	NP_006209.2:p.Arg683Thr
NM_006218.3:c.2048G>C	NP_006209.2:p.Arg683Thr
ENST00000263967.3:c.2048G>C	ENSP00000263967.3:p.Arg683Thr
ENST00000462255.1:n.322G>C
ENST00000462255.2:n.510G>C
ENST00000643187.1:c.2048G>C	ENSP00000493507.1:p.Arg683Thr
ENST00000674534.1:n.2956G>C
ENST00000674622.1:c.469G>C	ENSP00000502417.1:n.469G>C
ENST00000675467.1:n.4855G>C
ENST00000675786.1:c.*615G>C	ENSP00000502323.1:n.*615G>C
XM_006713658.2:c.2048G>C	XP_006713721.1:p.Arg683Thr
XM_006713658.4:c.2048G>C	XP_006713721.1:p.Arg683Thr
XM_011512894.1:c.2048G>C	XP_011511196.1:p.Arg683Thr
XM_011512894.2:c.2048G>C	XP_011511196.1:p.Arg683Thr