Canonical Allele Identifier: CA16602699

Gene: PIK3CA

Linked Data

• ClinVar Variation Id: 376246
• ClinVar RCV Id: RCV000426577 ; RCV001327967 ; RCV001851016
• dbSNP Id: rs121913288
• COSMIC: COSM12461 ; COSM276755
• MyVariant Identifiers: chr3:g.178952007A>G (hg19) ; chr3:g.179234219A>G (hg38)
• CIViC: CA16602699
• PubMed: PMID:25157968

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179234219A>G , CM000665.2:g.179234219A>G	GRCh38
NC_000003.11:g.178952007A>G , CM000665.1:g.178952007A>G	GRCh37
NC_000003.10:g.180434701A>G	NCBI36
NG_012113.2:g.90697A>G , LRG_310:g.90697A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.3062A>G MANE Select	ENSP00000263967.3:p.Tyr1021Cys
ENST00000462255.2:n.2085A>G
ENST00000643187.1:c.*142A>G	ENSP00000493507.1:n.*142A>G
ENST00000674534.1:n.3970A>G
ENST00000674622.1:c.1483A>G	ENSP00000502417.1:n.1483A>G
ENST00000675467.1:n.5869A>G
ENST00000675786.1:c.*1629A>G	ENSP00000502323.1:n.*1629A>G
ENST00000675796.1:n.2957A>G
ENST00000263967.3:c.3062A>G	ENSP00000263967.3:p.Tyr1021Cys
NM_006218.2:c.3062A>G , LRG_310t1:c.3062A>G	NP_006209.2:p.Tyr1021Cys
XM_006713658.2:c.3062A>G	XP_006713721.1:p.Tyr1021Cys
XM_011512894.1:c.3062A>G	XP_011511196.1:p.Tyr1021Cys
NM_006218.3:c.3062A>G	NP_006209.2:p.Tyr1021Cys
XM_006713658.4:c.3062A>G	XP_006713721.1:p.Tyr1021Cys
XM_011512894.2:c.3062A>G	XP_011511196.1:p.Tyr1021Cys
NM_006218.4:c.3062A>G MANE Select	NP_006209.2:p.Tyr1021Cys