Canonical Allele Identifier: CA355266097

Gene: PIK3CA

Linked Data

• MyVariant Identifiers: chr3:g.178937403G>T (hg19) ; chr3:g.179219615G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179219615G>T , CM000665.2:g.179219615G>T	GRCh38
NC_000003.11:g.178937403G>T , CM000665.1:g.178937403G>T	GRCh37
NC_000003.10:g.180420097G>T	NCBI36
NG_012113.2:g.76093G>T , LRG_310:g.76093G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.1791G>T MANE Select	ENSP00000263967.3:p.Gln597His
ENST00000462255.2:n.253G>T
ENST00000643187.1:c.1791G>T	ENSP00000493507.1:p.Gln597His
ENST00000674534.1:n.2699G>T
ENST00000674622.1:c.212G>T	ENSP00000502417.1:n.212G>T
ENST00000675467.1:n.4598G>T
ENST00000675786.1:c.*358G>T	ENSP00000502323.1:n.*358G>T
ENST00000263967.3:c.1791G>T	ENSP00000263967.3:p.Gln597His
ENST00000462255.1:n.65G>T
NM_006218.2:c.1791G>T , LRG_310t1:c.1791G>T	NP_006209.2:p.Gln597His
XM_006713658.2:c.1791G>T	XP_006713721.1:p.Gln597His
XM_011512894.1:c.1791G>T	XP_011511196.1:p.Gln597His
NM_006218.3:c.1791G>T	NP_006209.2:p.Gln597His
XM_006713658.4:c.1791G>T	XP_006713721.1:p.Gln597His
XM_011512894.2:c.1791G>T	XP_011511196.1:p.Gln597His
NM_006218.4:c.1791G>T MANE Select	NP_006209.2:p.Gln597His