Canonical Allele Identifier: CA355285846

Gene: PIK3CA

Linked Data

• dbSNP Id: rs2108429912
• gnomAD v4: 3-179234299-C-T
• COSMIC: COSM249875
• MyVariant Identifiers: chr3:g.178952087C>T (hg19) ; chr3:g.179234299C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179234299C>T , CM000665.2:g.179234299C>T	GRCh38
NC_000003.11:g.178952087C>T , CM000665.1:g.178952087C>T	GRCh37
NC_000003.10:g.180434781C>T	NCBI36
NG_012113.2:g.90777C>T , LRG_310:g.90777C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.3142C>T MANE Select	ENSP00000263967.3:p.His1048Tyr
ENST00000462255.2:n.2165C>T
ENST00000643187.1:c.*222C>T	ENSP00000493507.1:n.*222C>T
ENST00000674534.1:n.4050C>T
ENST00000674622.1:c.1563C>T	ENSP00000502417.1:n.1563C>T
ENST00000675467.1:n.5949C>T
ENST00000675786.1:c.*1709C>T	ENSP00000502323.1:n.*1709C>T
ENST00000675796.1:n.3037C>T
ENST00000263967.3:c.3142C>T	ENSP00000263967.3:p.His1048Tyr
NM_006218.2:c.3142C>T , LRG_310t1:c.3142C>T	NP_006209.2:p.His1048Tyr
XM_006713658.2:c.3142C>T	XP_006713721.1:p.His1048Tyr
XM_011512894.1:c.3142C>T	XP_011511196.1:p.His1048Tyr
NM_006218.3:c.3142C>T	NP_006209.2:p.His1048Tyr
XM_006713658.4:c.3142C>T	XP_006713721.1:p.His1048Tyr
XM_011512894.2:c.3142C>T	XP_011511196.1:p.His1048Tyr
NM_006218.4:c.3142C>T MANE Select	NP_006209.2:p.His1048Tyr