Canonical Allele Identifier: CA355285657

Gene: PIK3CA

Linked Data

• dbSNP Id: rs2108429680
• COSMIC: COSM3725191 ; COSM3725192
• MyVariant Identifiers: chr3:g.178952037C>G (hg19) ; chr3:g.179234249C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179234249C>G , CM000665.2:g.179234249C>G	GRCh38
NC_000003.11:g.178952037C>G , CM000665.1:g.178952037C>G	GRCh37
NC_000003.10:g.180434731C>G	NCBI36
NG_012113.2:g.90727C>G , LRG_310:g.90727C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.3092C>G MANE Select	ENSP00000263967.3:p.Thr1031Ser
ENST00000462255.2:n.2115C>G
ENST00000643187.1:c.*172C>G	ENSP00000493507.1:n.*172C>G
ENST00000674534.1:n.4000C>G
ENST00000674622.1:c.1513C>G	ENSP00000502417.1:n.1513C>G
ENST00000675467.1:n.5899C>G
ENST00000675786.1:c.*1659C>G	ENSP00000502323.1:n.*1659C>G
ENST00000675796.1:n.2987C>G
ENST00000263967.3:c.3092C>G	ENSP00000263967.3:p.Thr1031Ser
NM_006218.2:c.3092C>G , LRG_310t1:c.3092C>G	NP_006209.2:p.Thr1031Ser
XM_006713658.2:c.3092C>G	XP_006713721.1:p.Thr1031Ser
XM_011512894.1:c.3092C>G	XP_011511196.1:p.Thr1031Ser
NM_006218.3:c.3092C>G	NP_006209.2:p.Thr1031Ser
XM_006713658.4:c.3092C>G	XP_006713721.1:p.Thr1031Ser
XM_011512894.2:c.3092C>G	XP_011511196.1:p.Thr1031Ser
NM_006218.4:c.3092C>G MANE Select	NP_006209.2:p.Thr1031Ser