Canonical Allele Identifier: CA355285298

Gene: PIK3CA

Linked Data

• dbSNP Id: rs2108429440
• COSMIC: COSM27377 ; COSM304026
• MyVariant Identifiers: chr3:g.178951994G>C (hg19) ; chr3:g.179234206G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179234206G>C , CM000665.2:g.179234206G>C	GRCh38
NC_000003.11:g.178951994G>C , CM000665.1:g.178951994G>C	GRCh37
NC_000003.10:g.180434688G>C	NCBI36
NG_012113.2:g.90684G>C , LRG_310:g.90684G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000263967.4:c.3049G>C MANE Select	ENSP00000263967.3:p.Asp1017His
ENST00000462255.2:n.2072G>C
ENST00000643187.1:c.*129G>C	ENSP00000493507.1:n.*129G>C
ENST00000674534.1:n.3957G>C
ENST00000674622.1:c.1470G>C	ENSP00000502417.1:n.1470G>C
ENST00000675467.1:n.5856G>C
ENST00000675786.1:c.*1616G>C	ENSP00000502323.1:n.*1616G>C
ENST00000675796.1:n.2944G>C
ENST00000263967.3:c.3049G>C	ENSP00000263967.3:p.Asp1017His
NM_006218.2:c.3049G>C , LRG_310t1:c.3049G>C	NP_006209.2:p.Asp1017His
XM_006713658.2:c.3049G>C	XP_006713721.1:p.Asp1017His
XM_011512894.1:c.3049G>C	XP_011511196.1:p.Asp1017His
NM_006218.3:c.3049G>C	NP_006209.2:p.Asp1017His
XM_006713658.4:c.3049G>C	XP_006713721.1:p.Asp1017His
XM_011512894.2:c.3049G>C	XP_011511196.1:p.Asp1017His
NM_006218.4:c.3049G>C MANE Select	NP_006209.2:p.Asp1017His