Canonical Allele Identifier: CA437316051

Gene: PIK3CA

Linked Data

• dbSNP Id: rs1724483318
• COSMIC: COSM1041472 ; COSM1041473
• MyVariant Identifiers: chr3:g.178921544C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179203756C>A , CM000665.2:g.179203756C>A	GRCh38
NC_000003.11:g.178921544C>A , CM000665.1:g.178921544C>A	GRCh37
NC_000003.10:g.180404238C>A	NCBI36
NG_012113.2:g.60234C>A , LRG_310:g.60234C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.1026C>A MANE Select	ENSP00000263967.3:p.Thr342=
ENST00000643187.1:c.1026C>A	ENSP00000493507.1:p.Thr342=
ENST00000674534.1:n.780C>A
ENST00000675467.1:n.3833C>A
ENST00000675786.1:c.1026C>A	ENSP00000502323.1:p.Thr342=
ENST00000263967.3:c.1026C>A	ENSP00000263967.3:p.Thr342=
NM_006218.2:c.1026C>A , LRG_310t1:c.1026C>A	NP_006209.2:p.Thr342=
XM_006713658.2:c.1026C>A	XP_006713721.1:p.Thr342=
XM_011512894.1:c.1026C>A	XP_011511196.1:p.Thr342=
NM_006218.3:c.1026C>A	NP_006209.2:p.Thr342=
XM_006713658.4:c.1026C>A	XP_006713721.1:p.Thr342=
XM_011512894.2:c.1026C>A	XP_011511196.1:p.Thr342=
NM_006218.4:c.1026C>A MANE Select	NP_006209.2:p.Thr342=