Canonical Allele Identifier: CA355285420

Gene: PIK3CA

Linked Data

• ClinVar Variation Id: 1691391
• ClinVar RCV Id: RCV003157111
• dbSNP Id: rs2108429509
• COSMIC: COSM17444 ; COSM246589
• MyVariant Identifiers: chr3:g.178952006T>C (hg19) ; chr3:g.179234218T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179234218T>C , CM000665.2:g.179234218T>C	GRCh38
NC_000003.11:g.178952006T>C , CM000665.1:g.178952006T>C	GRCh37
NC_000003.10:g.180434700T>C	NCBI36
NG_012113.2:g.90696T>C , LRG_310:g.90696T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.3061T>C MANE Select	ENSP00000263967.3:p.Tyr1021His
ENST00000462255.2:n.2084T>C
ENST00000643187.1:c.*141T>C	ENSP00000493507.1:n.*141T>C
ENST00000674534.1:n.3969T>C
ENST00000674622.1:c.1482T>C	ENSP00000502417.1:n.1482T>C
ENST00000675467.1:n.5868T>C
ENST00000675786.1:c.*1628T>C	ENSP00000502323.1:n.*1628T>C
ENST00000675796.1:n.2956T>C
ENST00000263967.3:c.3061T>C	ENSP00000263967.3:p.Tyr1021His
NM_006218.2:c.3061T>C , LRG_310t1:c.3061T>C	NP_006209.2:p.Tyr1021His
XM_006713658.2:c.3061T>C	XP_006713721.1:p.Tyr1021His
XM_011512894.1:c.3061T>C	XP_011511196.1:p.Tyr1021His
NM_006218.3:c.3061T>C	NP_006209.2:p.Tyr1021His
XM_006713658.4:c.3061T>C	XP_006713721.1:p.Tyr1021His
XM_011512894.2:c.3061T>C	XP_011511196.1:p.Tyr1021His
NM_006218.4:c.3061T>C MANE Select	NP_006209.2:p.Tyr1021His