Canonical Allele Identifier: CA16602904

Gene: PIK3CA

Linked Data

• ClinVar Variation Id: 376470
• ClinVar RCV Id: RCV001327961 ; RCV001526693 ; RCV001775789 ; RCV001861479 ; RCV002244865 ; RCV002472374
• dbSNP Id: rs1057519925
• COSMIC: COSM12584 ; COSM446007
• MyVariant Identifiers: chr3:g.178928079G>A (hg19) ; chr3:g.179210291G>A (hg38)
• PubMed: PMID:26619011

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179210291G>A , CM000665.2:g.179210291G>A	GRCh38
NC_000003.11:g.178928079G>A , CM000665.1:g.178928079G>A	GRCh37
NC_000003.10:g.180410773G>A	NCBI36
NG_012113.2:g.66769G>A , LRG_310:g.66769G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000263967.4:c.1357G>A MANE Select	ENSP00000263967.3:p.Glu453Lys
ENST00000643187.1:c.1357G>A	ENSP00000493507.1:p.Glu453Lys
ENST00000674534.1:n.1111G>A
ENST00000675467.1:n.4164G>A
ENST00000675786.1:c.1357G>A	ENSP00000502323.1:p.Glu453Lys
ENST00000263967.3:c.1357G>A	ENSP00000263967.3:p.Glu453Lys
NM_006218.2:c.1357G>A , LRG_310t1:c.1357G>A	NP_006209.2:p.Glu453Lys
XM_006713658.2:c.1357G>A	XP_006713721.1:p.Glu453Lys
XM_011512894.1:c.1357G>A	XP_011511196.1:p.Glu453Lys
NM_006218.3:c.1357G>A	NP_006209.2:p.Glu453Lys
XM_006713658.4:c.1357G>A	XP_006713721.1:p.Glu453Lys
XM_011512894.2:c.1357G>A	XP_011511196.1:p.Glu453Lys
NM_006218.4:c.1357G>A MANE Select	NP_006209.2:p.Glu453Lys