Canonical Allele Identifier: CA180900
Gene: PIK3CA HGNC NCBI

Linked Data

ClinVar Variation Id: 31945
ClinVar RCV Id: RCV000024623 RCV000154512 RCV000201232 RCV000423306 RCV000427443 RCV000433143 RCV000434659 RCV000439612 RCV000444019 RCV000444813 RCV000709694 RCV001327960 RCV001526612 RCV001705599 RCV002054475 RCV003588566
dbSNP Id: rs121913272
COSMIC: COSM757 COSM267862
MyVariant Identifiers: chr3:g.178927980T>C (hg19) chr3:g.179210192T>C (hg38)
CIViC: CA180900
PubMed: PMID:15016963 PMID:15520168 PMID:18183466 PMID:22658544 PMID:23946963 PMID:25157968 PMID:26619011
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179210192T>C , CM000665.2:g.179210192T>C GRCh38
NC_000003.11:g.178927980T>C , CM000665.1:g.178927980T>C GRCh37
NC_000003.10:g.180410674T>C NCBI36
NG_012113.2:g.66670T>C , LRG_310:g.66670T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000263967.4:c.1258T>C MANE Select ENSP00000263967.3:p.Cys420Arg
ENST00000643187.1:c.1258T>C ENSP00000493507.1:p.Cys420Arg
ENST00000674534.1:n.1012T>C
ENST00000675467.1:n.4065T>C
ENST00000675786.1:c.1258T>C ENSP00000502323.1:p.Cys420Arg
ENST00000263967.3:c.1258T>C ENSP00000263967.3:p.Cys420Arg
NM_006218.2:c.1258T>C , LRG_310t1:c.1258T>C NP_006209.2:p.Cys420Arg
XM_006713658.2:c.1258T>C XP_006713721.1:p.Cys420Arg
XM_011512894.1:c.1258T>C XP_011511196.1:p.Cys420Arg
NM_006218.3:c.1258T>C NP_006209.2:p.Cys420Arg
XM_006713658.4:c.1258T>C XP_006713721.1:p.Cys420Arg
XM_011512894.2:c.1258T>C XP_011511196.1:p.Cys420Arg
NM_006218.4:c.1258T>C MANE Select NP_006209.2:p.Cys420Arg
Search 100 bp 5'
Search 100 bp 3'