Canonical Allele Identifier: CA210107

Gene: PIK3CA

Linked Data

• ClinVar Variation Id: 217292
• ClinVar RCV Id: RCV000201236 ; RCV000442578 ; RCV000631214 ; RCV003320599
• dbSNP Id: rs121913283
• COSMIC: COSM773 ; COSM419700
• MyVariant Identifiers: chr3:g.178952074G>T (hg19) ; chr3:g.179234286G>T (hg38)
• CIViC: CA210107
• PubMed: PMID:15930273 ; PMID:25157968

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179234286G>T , CM000665.2:g.179234286G>T	GRCh38
NC_000003.11:g.178952074G>T , CM000665.1:g.178952074G>T	GRCh37
NC_000003.10:g.180434768G>T	NCBI36
NG_012113.2:g.90764G>T , LRG_310:g.90764G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.3129G>T MANE Select	ENSP00000263967.3:p.Met1043Ile
ENST00000462255.2:n.2152G>T
ENST00000643187.1:c.*209G>T	ENSP00000493507.1:n.*209G>T
ENST00000674534.1:n.4037G>T
ENST00000674622.1:c.1550G>T	ENSP00000502417.1:n.1550G>T
ENST00000675467.1:n.5936G>T
ENST00000675786.1:c.*1696G>T	ENSP00000502323.1:n.*1696G>T
ENST00000675796.1:n.3024G>T
ENST00000263967.3:c.3129G>T	ENSP00000263967.3:p.Met1043Ile
NM_006218.2:c.3129G>T , LRG_310t1:c.3129G>T	NP_006209.2:p.Met1043Ile
XM_006713658.2:c.3129G>T	XP_006713721.1:p.Met1043Ile
XM_011512894.1:c.3129G>T	XP_011511196.1:p.Met1043Ile
NM_006218.3:c.3129G>T	NP_006209.2:p.Met1043Ile
XM_006713658.4:c.3129G>T	XP_006713721.1:p.Met1043Ile
XM_011512894.2:c.3129G>T	XP_011511196.1:p.Met1043Ile
NM_006218.4:c.3129G>T MANE Select	NP_006209.2:p.Met1043Ile