Canonical Allele Identifier: CA355270382

Gene: PIK3CA

Linked Data

• dbSNP Id: rs2108385056
• MyVariant Identifiers: chr3:g.178916645G>A (hg19) ; chr3:g.179198857G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179198857G>A , CM000665.2:g.179198857G>A	GRCh38
NC_000003.11:g.178916645G>A , CM000665.1:g.178916645G>A	GRCh37
NC_000003.10:g.180399339G>A	NCBI36
NG_012113.2:g.55335G>A , LRG_310:g.55335G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.32G>A MANE Select	ENSP00000263967.3:p.Trp11Ter
ENST00000643187.1:c.32G>A	ENSP00000493507.1:p.Trp11Ter
ENST00000675467.1:n.2839G>A
ENST00000675786.1:c.32G>A	ENSP00000502323.1:p.Trp11Ter
ENST00000263967.3:c.32G>A	ENSP00000263967.3:p.Trp11Ter
ENST00000468036.1:c.32G>A	ENSP00000417479.1:p.Trp11Ter
ENST00000477735.1:c.32G>A	ENSP00000418145.1:p.Trp11Ter
NM_006218.2:c.32G>A , LRG_310t1:c.32G>A	NP_006209.2:p.Trp11Ter
XM_006713658.2:c.32G>A	XP_006713721.1:p.Trp11Ter
XM_011512894.1:c.32G>A	XP_011511196.1:p.Trp11Ter
NM_006218.3:c.32G>A	NP_006209.2:p.Trp11Ter
XM_006713658.4:c.32G>A	XP_006713721.1:p.Trp11Ter
XM_011512894.2:c.32G>A	XP_011511196.1:p.Trp11Ter
NM_006218.4:c.32G>A MANE Select	NP_006209.2:p.Trp11Ter