Canonical Allele Identifier: CA355271192

Gene: PIK3CA

Linked Data

• MyVariant Identifiers: chr3:g.178916730G>T (hg19) ; chr3:g.179198942G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179198942G>T , CM000665.2:g.179198942G>T	GRCh38
NC_000003.11:g.178916730G>T , CM000665.1:g.178916730G>T	GRCh37
NC_000003.10:g.180399424G>T	NCBI36
NG_012113.2:g.55420G>T , LRG_310:g.55420G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000263967.4:c.117G>T MANE Select	ENSP00000263967.3:p.Glu39Asp
ENST00000643187.1:c.117G>T	ENSP00000493507.1:p.Glu39Asp
ENST00000675467.1:n.2924G>T
ENST00000675786.1:c.117G>T	ENSP00000502323.1:p.Glu39Asp
ENST00000263967.3:c.117G>T	ENSP00000263967.3:p.Glu39Asp
ENST00000468036.1:c.117G>T	ENSP00000417479.1:p.Glu39Asp
NM_006218.2:c.117G>T , LRG_310t1:c.117G>T	NP_006209.2:p.Glu39Asp
XM_006713658.2:c.117G>T	XP_006713721.1:p.Glu39Asp
XM_011512894.1:c.117G>T	XP_011511196.1:p.Glu39Asp
NM_006218.3:c.117G>T	NP_006209.2:p.Glu39Asp
XM_006713658.4:c.117G>T	XP_006713721.1:p.Glu39Asp
XM_011512894.2:c.117G>T	XP_011511196.1:p.Glu39Asp
NM_006218.4:c.117G>T MANE Select	NP_006209.2:p.Glu39Asp