Canonical Allele Identifier: CA16611386

Gene: PIK3CA

Linked Data

• ClinVar Variation Id: 403910
• ClinVar RCV Id: RCV000467076
• dbSNP Id: rs1060500028
• MyVariant Identifiers: chr3:g.178937378A>G (hg19) ; chr3:g.179219590A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179219590A>G , CM000665.2:g.179219590A>G	GRCh38
NC_000003.11:g.178937378A>G , CM000665.1:g.178937378A>G	GRCh37
NC_000003.10:g.180420072A>G	NCBI36
NG_012113.2:g.76068A>G , LRG_310:g.76068A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.1766A>G MANE Select	ENSP00000263967.3:p.Asp589Gly
ENST00000462255.2:n.228A>G
ENST00000643187.1:c.1766A>G	ENSP00000493507.1:p.Asp589Gly
ENST00000674534.1:n.2674A>G
ENST00000674622.1:c.187A>G	ENSP00000502417.1:n.187A>G
ENST00000675467.1:n.4573A>G
ENST00000675786.1:c.*333A>G	ENSP00000502323.1:n.*333A>G
ENST00000263967.3:c.1766A>G	ENSP00000263967.3:p.Asp589Gly
ENST00000462255.1:n.40A>G
NM_006218.2:c.1766A>G , LRG_310t1:c.1766A>G	NP_006209.2:p.Asp589Gly
XM_006713658.2:c.1766A>G	XP_006713721.1:p.Asp589Gly
XM_011512894.1:c.1766A>G	XP_011511196.1:p.Asp589Gly
NM_006218.3:c.1766A>G	NP_006209.2:p.Asp589Gly
XM_006713658.4:c.1766A>G	XP_006713721.1:p.Asp589Gly
XM_011512894.2:c.1766A>G	XP_011511196.1:p.Asp589Gly
NM_006218.4:c.1766A>G MANE Select	NP_006209.2:p.Asp589Gly