Canonical Allele Identifier: CA355285392

Gene: PIK3CA

Linked Data

• dbSNP Id: rs2108429501
• COSMIC: COSM6475717 ; COSM6475718
• MyVariant Identifiers: chr3:g.178952003G>A (hg19) ; chr3:g.179234215G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179234215G>A , CM000665.2:g.179234215G>A	GRCh38
NC_000003.11:g.178952003G>A , CM000665.1:g.178952003G>A	GRCh37
NC_000003.10:g.180434697G>A	NCBI36
NG_012113.2:g.90693G>A , LRG_310:g.90693G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000263967.4:c.3058G>A MANE Select	ENSP00000263967.3:p.Ala1020Thr
ENST00000462255.2:n.2081G>A
ENST00000643187.1:c.*138G>A	ENSP00000493507.1:n.*138G>A
ENST00000674534.1:n.3966G>A
ENST00000674622.1:c.1479G>A	ENSP00000502417.1:n.1479G>A
ENST00000675467.1:n.5865G>A
ENST00000675786.1:c.*1625G>A	ENSP00000502323.1:n.*1625G>A
ENST00000675796.1:n.2953G>A
ENST00000263967.3:c.3058G>A	ENSP00000263967.3:p.Ala1020Thr
NM_006218.2:c.3058G>A , LRG_310t1:c.3058G>A	NP_006209.2:p.Ala1020Thr
XM_006713658.2:c.3058G>A	XP_006713721.1:p.Ala1020Thr
XM_011512894.1:c.3058G>A	XP_011511196.1:p.Ala1020Thr
NM_006218.3:c.3058G>A	NP_006209.2:p.Ala1020Thr
XM_006713658.4:c.3058G>A	XP_006713721.1:p.Ala1020Thr
XM_011512894.2:c.3058G>A	XP_011511196.1:p.Ala1020Thr
NM_006218.4:c.3058G>A MANE Select	NP_006209.2:p.Ala1020Thr