Canonical Allele Identifier: CA355265091

Gene: PIK3CA

Linked Data

• dbSNP Id: rs1057519940
• COSMIC: COSM5881064 ; COSM5881065
• MyVariant Identifiers: chr3:g.178936096G>C (hg19) ; chr3:g.179218308G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179218308G>C , CM000665.2:g.179218308G>C	GRCh38
NC_000003.11:g.178936096G>C , CM000665.1:g.178936096G>C	GRCh37
NC_000003.10:g.180418790G>C	NCBI36
NG_012113.2:g.74786G>C , LRG_310:g.74786G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.1638G>C MANE Select	ENSP00000263967.3:p.Gln546His
ENST00000462255.2:n.100G>C
ENST00000643187.1:c.1638G>C	ENSP00000493507.1:p.Gln546His
ENST00000674534.1:n.1392G>C
ENST00000674622.1:c.141G>C	ENSP00000502417.1:p.Gln47His
ENST00000675467.1:n.4445G>C
ENST00000675786.1:c.*205G>C	ENSP00000502323.1:n.*205G>C
ENST00000263967.3:c.1638G>C	ENSP00000263967.3:p.Gln546His
NM_006218.2:c.1638G>C , LRG_310t1:c.1638G>C	NP_006209.2:p.Gln546His
XM_006713658.2:c.1638G>C	XP_006713721.1:p.Gln546His
XM_011512894.1:c.1638G>C	XP_011511196.1:p.Gln546His
NM_006218.3:c.1638G>C	NP_006209.2:p.Gln546His
XM_006713658.4:c.1638G>C	XP_006713721.1:p.Gln546His
XM_011512894.2:c.1638G>C	XP_011511196.1:p.Gln546His
NM_006218.4:c.1638G>C MANE Select	NP_006209.2:p.Gln546His