Canonical Allele Identifier: CA2710881

Gene: PIK3CA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179221160G>A , CM000665.2:g.179221160G>A	GRCh38
NC_000003.11:g.178938948G>A , CM000665.1:g.178938948G>A	GRCh37
NC_000003.10:g.180421642G>A	NCBI36
NG_012113.2:g.77638G>A , LRG_310:g.77638G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.2187+3G>A MANE Select	ENSP00000263967.3:n.2187+3G>A
ENST00000462255.2:n.649+3G>A
ENST00000643187.1:c.2187+3G>A	ENSP00000493507.1:n.2187+3G>A
ENST00000674534.1:n.3095+3G>A
ENST00000674622.1:c.608+3G>A	ENSP00000502417.1:n.608+3G>A
ENST00000675467.1:n.4994+3G>A
ENST00000675786.1:c.*754+3G>A	ENSP00000502323.1:n.*754+3G>A
ENST00000263967.3:c.2187+3G>A	ENSP00000263967.3:n.2187+3G>A
ENST00000462255.1:n.461+3G>A
NM_006218.2:c.2187+3G>A , LRG_310t1:c.2187+3G>A	NP_006209.2:n.2187+3G>A
XM_006713658.2:c.2187+3G>A	XP_006713721.1:n.2187+3G>A
XM_011512894.1:c.2187+3G>A	XP_011511196.1:n.2187+3G>A
NM_006218.3:c.2187+3G>A	NP_006209.2:n.2187+3G>A
XM_006713658.4:c.2187+3G>A	XP_006713721.1:n.2187+3G>A
XM_011512894.2:c.2187+3G>A	XP_011511196.1:n.2187+3G>A
NM_006218.4:c.2187+3G>A MANE Select	NP_006209.2:n.2187+3G>A