Canonical Allele Identifier: CA437316005

Gene: PIK3CA

Linked Data

• MyVariant Identifiers: chr3:g.178916871A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179199083A>T , CM000665.2:g.179199083A>T	GRCh38
NC_000003.11:g.178916871A>T , CM000665.1:g.178916871A>T	GRCh37
NC_000003.10:g.180399565A>T	NCBI36
NG_012113.2:g.55561A>T , LRG_310:g.55561A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.258A>T MANE Select	ENSP00000263967.3:p.Thr86=
ENST00000643187.1:c.258A>T	ENSP00000493507.1:p.Thr86=
ENST00000675467.1:n.3065A>T
ENST00000675786.1:c.258A>T	ENSP00000502323.1:p.Thr86=
ENST00000263967.3:c.258A>T	ENSP00000263967.3:p.Thr86=
ENST00000468036.1:c.258A>T	ENSP00000417479.1:p.Thr86=
NM_006218.2:c.258A>T , LRG_310t1:c.258A>T	NP_006209.2:p.Thr86=
XM_006713658.2:c.258A>T	XP_006713721.1:p.Thr86=
XM_011512894.1:c.258A>T	XP_011511196.1:p.Thr86=
NM_006218.3:c.258A>T	NP_006209.2:p.Thr86=
XM_006713658.4:c.258A>T	XP_006713721.1:p.Thr86=
XM_011512894.2:c.258A>T	XP_011511196.1:p.Thr86=
NM_006218.4:c.258A>T MANE Select	NP_006209.2:p.Thr86=