Canonical Allele Identifier: CA88525428

Gene: PIK3CA

Linked Data

• dbSNP Id: rs769884883
• MyVariant Identifiers: chr3:g.178932558_178932559insTT (hg19) ; chr3:g.179214770_179214771insTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179214771_179214772dup , CM000665.2:g.179214771_179214772dup	GRCh38
NC_000003.11:g.178932559_178932560dup , CM000665.1:g.178932559_178932560dup	GRCh37
NC_000003.10:g.180415253_180415254dup	NCBI36
NG_012113.2:g.71249_71250dup , LRG_310:g.71249_71250dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.1540-3439_1540-3438dup MANE Select	ENSP00000263967.3:n.1540-3439_1540-3438dup
ENST00000643187.1:c.1540-3439_1540-3438dup	ENSP00000493507.1:n.1540-3439_1540-3438dup
ENST00000674534.1:n.1294-3439_1294-3438dup
ENST00000674622.1:c.43-3439_43-3438dup	ENSP00000502417.1:n.43-3439_43-3438dup
ENST00000675467.1:n.4347-3439_4347-3438dup
ENST00000675786.1:c.*107-3439_*107-3438dup	ENSP00000502323.1:n.*107-3439_*107-3438dup
ENST00000263967.3:c.1540-3439_1540-3438dup	ENSP00000263967.3:n.1540-3439_1540-3438dup
NM_006218.2:c.1540-3439_1540-3438dup , LRG_310t1:c.1540-3439_1540-3438dup	NP_006209.2:n.1540-3439_1540-3438dup
XM_006713658.2:c.1540-3439_1540-3438dup	XP_006713721.1:n.1540-3439_1540-3438dup
XM_011512894.1:c.1540-3439_1540-3438dup	XP_011511196.1:n.1540-3439_1540-3438dup
NM_006218.3:c.1540-3439_1540-3438dup	NP_006209.2:n.1540-3439_1540-3438dup
XM_006713658.4:c.1540-3439_1540-3438dup	XP_006713721.1:n.1540-3439_1540-3438dup
XM_011512894.2:c.1540-3439_1540-3438dup	XP_011511196.1:n.1540-3439_1540-3438dup
NM_006218.4:c.1540-3439_1540-3438dup MANE Select	NP_006209.2:n.1540-3439_1540-3438dup