Canonical Allele Identifier: CA355285307

Gene: PIK3CA

Linked Data

• ClinVar Variation Id: 2630970
• ClinVar RCV Id: RCV003404344
• dbSNP Id: rs2108429450
• COSMIC: COSM328024
• MyVariant Identifiers: chr3:g.178951995A>T (hg19) ; chr3:g.179234207A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179234207A>T , CM000665.2:g.179234207A>T	GRCh38
NC_000003.11:g.178951995A>T , CM000665.1:g.178951995A>T	GRCh37
NC_000003.10:g.180434689A>T	NCBI36
NG_012113.2:g.90685A>T , LRG_310:g.90685A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000263967.4:c.3050A>T MANE Select	ENSP00000263967.3:p.Asp1017Val
ENST00000462255.2:n.2073A>T
ENST00000643187.1:c.*130A>T	ENSP00000493507.1:n.*130A>T
ENST00000674534.1:n.3958A>T
ENST00000674622.1:c.1471A>T	ENSP00000502417.1:n.1471A>T
ENST00000675467.1:n.5857A>T
ENST00000675786.1:c.*1617A>T	ENSP00000502323.1:n.*1617A>T
ENST00000675796.1:n.2945A>T
ENST00000263967.3:c.3050A>T	ENSP00000263967.3:p.Asp1017Val
NM_006218.2:c.3050A>T , LRG_310t1:c.3050A>T	NP_006209.2:p.Asp1017Val
XM_006713658.2:c.3050A>T	XP_006713721.1:p.Asp1017Val
XM_011512894.1:c.3050A>T	XP_011511196.1:p.Asp1017Val
NM_006218.3:c.3050A>T	NP_006209.2:p.Asp1017Val
XM_006713658.4:c.3050A>T	XP_006713721.1:p.Asp1017Val
XM_011512894.2:c.3050A>T	XP_011511196.1:p.Asp1017Val
NM_006218.4:c.3050A>T MANE Select	NP_006209.2:p.Asp1017Val