Canonical Allele Identifier: CA16602195

Gene: PIK3CA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179234169G>A , CM000665.2:g.179234169G>A	GRCh38
NC_000003.11:g.178951957G>A , CM000665.1:g.178951957G>A	GRCh37
NC_000003.10:g.180434651G>A	NCBI36
NG_012113.2:g.90647G>A , LRG_310:g.90647G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_006218.4:c.3012G>A MANE Select	NP_006209.2:p.Met1004Ile
ENST00000263967.4:c.3012G>A MANE Select	ENSP00000263967.3:p.Met1004Ile
NM_006218.2:c.3012G>A , LRG_310t1:c.3012G>A	NP_006209.2:p.Met1004Ile
NM_006218.3:c.3012G>A	NP_006209.2:p.Met1004Ile
ENST00000263967.3:c.3012G>A	ENSP00000263967.3:p.Met1004Ile
ENST00000462255.2:n.2035G>A
ENST00000643187.1:c.*92G>A	ENSP00000493507.1:n.*92G>A
ENST00000674534.1:n.3920G>A
ENST00000674622.1:c.1433G>A	ENSP00000502417.1:n.1433G>A
ENST00000675467.1:n.5819G>A
ENST00000675786.1:c.*1579G>A	ENSP00000502323.1:n.*1579G>A
ENST00000675796.1:n.2907G>A
XM_006713658.2:c.3012G>A	XP_006713721.1:p.Met1004Ile
XM_006713658.4:c.3012G>A	XP_006713721.1:p.Met1004Ile
XM_011512894.1:c.3012G>A	XP_011511196.1:p.Met1004Ile
XM_011512894.2:c.3012G>A	XP_011511196.1:p.Met1004Ile