Canonical Allele Identifier: CA355264493

Gene: PIK3CA

Linked Data

• dbSNP Id: rs2108407931
• MyVariant Identifiers: chr3:g.178936005G>C (hg19) ; chr3:g.179218217G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179218217G>C , CM000665.2:g.179218217G>C	GRCh38
NC_000003.11:g.178936005G>C , CM000665.1:g.178936005G>C	GRCh37
NC_000003.10:g.180418699G>C	NCBI36
NG_012113.2:g.74695G>C , LRG_310:g.74695G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000263967.4:c.1547G>C MANE Select	ENSP00000263967.3:p.Arg516Thr
ENST00000462255.2:n.9G>C
ENST00000643187.1:c.1547G>C	ENSP00000493507.1:p.Arg516Thr
ENST00000674534.1:n.1301G>C
ENST00000674622.1:c.50G>C	ENSP00000502417.1:p.Arg17Thr
ENST00000675467.1:n.4354G>C
ENST00000675786.1:c.*114G>C	ENSP00000502323.1:n.*114G>C
ENST00000263967.3:c.1547G>C	ENSP00000263967.3:p.Arg516Thr
NM_006218.2:c.1547G>C , LRG_310t1:c.1547G>C	NP_006209.2:p.Arg516Thr
XM_006713658.2:c.1547G>C	XP_006713721.1:p.Arg516Thr
XM_011512894.1:c.1547G>C	XP_011511196.1:p.Arg516Thr
NM_006218.3:c.1547G>C	NP_006209.2:p.Arg516Thr
XM_006713658.4:c.1547G>C	XP_006713721.1:p.Arg516Thr
XM_011512894.2:c.1547G>C	XP_011511196.1:p.Arg516Thr
NM_006218.4:c.1547G>C MANE Select	NP_006209.2:p.Arg516Thr