Canonical Allele Identifier: CA355265060

Gene: PIK3CA

Linked Data

• ClinVar Variation Id: 1504953
• ClinVar RCV Id: RCV002029173
• dbSNP Id: rs2108408335
• MyVariant Identifiers: chr3:g.178936089C>G (hg19) ; chr3:g.179218301C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179218301C>G , CM000665.2:g.179218301C>G	GRCh38
NC_000003.11:g.178936089C>G , CM000665.1:g.178936089C>G	GRCh37
NC_000003.10:g.180418783C>G	NCBI36
NG_012113.2:g.74779C>G , LRG_310:g.74779C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.1631C>G MANE Select	ENSP00000263967.3:p.Thr544Ser
ENST00000462255.2:n.93C>G
ENST00000643187.1:c.1631C>G	ENSP00000493507.1:p.Thr544Ser
ENST00000674534.1:n.1385C>G
ENST00000674622.1:c.134C>G	ENSP00000502417.1:p.Thr45Ser
ENST00000675467.1:n.4438C>G
ENST00000675786.1:c.*198C>G	ENSP00000502323.1:n.*198C>G
ENST00000263967.3:c.1631C>G	ENSP00000263967.3:p.Thr544Ser
NM_006218.2:c.1631C>G , LRG_310t1:c.1631C>G	NP_006209.2:p.Thr544Ser
XM_006713658.2:c.1631C>G	XP_006713721.1:p.Thr544Ser
XM_011512894.1:c.1631C>G	XP_011511196.1:p.Thr544Ser
NM_006218.3:c.1631C>G	NP_006209.2:p.Thr544Ser
XM_006713658.4:c.1631C>G	XP_006713721.1:p.Thr544Ser
XM_011512894.2:c.1631C>G	XP_011511196.1:p.Thr544Ser
NM_006218.4:c.1631C>G MANE Select	NP_006209.2:p.Thr544Ser