Canonical Allele Identifier: CA355270292

Gene: PIK3CA

Linked Data

• dbSNP Id: rs2108385018
• COSMIC: COSM3205590 ; COSM3205591
• MyVariant Identifiers: chr3:g.178916636G>A (hg19) ; chr3:g.179198848G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179198848G>A , CM000665.2:g.179198848G>A	GRCh38
NC_000003.11:g.178916636G>A , CM000665.1:g.178916636G>A	GRCh37
NC_000003.10:g.180399330G>A	NCBI36
NG_012113.2:g.55326G>A , LRG_310:g.55326G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000263967.4:c.23G>A MANE Select	ENSP00000263967.3:p.Gly8Asp
ENST00000643187.1:c.23G>A	ENSP00000493507.1:p.Gly8Asp
ENST00000675467.1:n.2830G>A
ENST00000675786.1:c.23G>A	ENSP00000502323.1:p.Gly8Asp
ENST00000263967.3:c.23G>A	ENSP00000263967.3:p.Gly8Asp
ENST00000468036.1:c.23G>A	ENSP00000417479.1:p.Gly8Asp
ENST00000477735.1:c.23G>A	ENSP00000418145.1:p.Gly8Asp
NM_006218.2:c.23G>A , LRG_310t1:c.23G>A	NP_006209.2:p.Gly8Asp
XM_006713658.2:c.23G>A	XP_006713721.1:p.Gly8Asp
XM_011512894.1:c.23G>A	XP_011511196.1:p.Gly8Asp
NM_006218.3:c.23G>A	NP_006209.2:p.Gly8Asp
XM_006713658.4:c.23G>A	XP_006713721.1:p.Gly8Asp
XM_011512894.2:c.23G>A	XP_011511196.1:p.Gly8Asp
NM_006218.4:c.23G>A MANE Select	NP_006209.2:p.Gly8Asp