Canonical Allele Identifier: CA355284746

Gene: PIK3CA

Linked Data

• MyVariant Identifiers: chr3:g.178951937T>C (hg19) ; chr3:g.179234149T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179234149T>C , CM000665.2:g.179234149T>C	GRCh38
NC_000003.11:g.178951937T>C , CM000665.1:g.178951937T>C	GRCh37
NC_000003.10:g.180434631T>C	NCBI36
NG_012113.2:g.90627T>C , LRG_310:g.90627T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.2992T>C MANE Select	ENSP00000263967.3:p.Phe998Leu
ENST00000462255.2:n.2015T>C
ENST00000643187.1:c.*72T>C	ENSP00000493507.1:n.*72T>C
ENST00000674534.1:n.3900T>C
ENST00000674622.1:c.1413T>C	ENSP00000502417.1:n.1413T>C
ENST00000675467.1:n.5799T>C
ENST00000675786.1:c.*1559T>C	ENSP00000502323.1:n.*1559T>C
ENST00000675796.1:n.2887T>C
ENST00000263967.3:c.2992T>C	ENSP00000263967.3:p.Phe998Leu
NM_006218.2:c.2992T>C , LRG_310t1:c.2992T>C	NP_006209.2:p.Phe998Leu
XM_006713658.2:c.2992T>C	XP_006713721.1:p.Phe998Leu
XM_011512894.1:c.2992T>C	XP_011511196.1:p.Phe998Leu
NM_006218.3:c.2992T>C	NP_006209.2:p.Phe998Leu
XM_006713658.4:c.2992T>C	XP_006713721.1:p.Phe998Leu
XM_011512894.2:c.2992T>C	XP_011511196.1:p.Phe998Leu
NM_006218.4:c.2992T>C MANE Select	NP_006209.2:p.Phe998Leu