Canonical Allele Identifier: CA355285877

Gene: PIK3CA

Linked Data

• dbSNP Id: rs2108429956
• MyVariant Identifiers: chr3:g.178952100C>G (hg19) ; chr3:g.179234312C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179234312C>G , CM000665.2:g.179234312C>G	GRCh38
NC_000003.11:g.178952100C>G , CM000665.1:g.178952100C>G	GRCh37
NC_000003.10:g.180434794C>G	NCBI36
NG_012113.2:g.90790C>G , LRG_310:g.90790C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000263967.4:c.3155C>G MANE Select	ENSP00000263967.3:p.Thr1052Arg
ENST00000462255.2:n.2178C>G
ENST00000643187.1:c.*235C>G	ENSP00000493507.1:n.*235C>G
ENST00000674534.1:n.4063C>G
ENST00000674622.1:c.1576C>G	ENSP00000502417.1:n.1576C>G
ENST00000675467.1:n.5962C>G
ENST00000675786.1:c.*1722C>G	ENSP00000502323.1:n.*1722C>G
ENST00000675796.1:n.3050C>G
ENST00000263967.3:c.3155C>G	ENSP00000263967.3:p.Thr1052Arg
NM_006218.2:c.3155C>G , LRG_310t1:c.3155C>G	NP_006209.2:p.Thr1052Arg
XM_006713658.2:c.3155C>G	XP_006713721.1:p.Thr1052Arg
XM_011512894.1:c.3155C>G	XP_011511196.1:p.Thr1052Arg
NM_006218.3:c.3155C>G	NP_006209.2:p.Thr1052Arg
XM_006713658.4:c.3155C>G	XP_006713721.1:p.Thr1052Arg
XM_011512894.2:c.3155C>G	XP_011511196.1:p.Thr1052Arg
NM_006218.4:c.3155C>G MANE Select	NP_006209.2:p.Thr1052Arg