Canonical Allele Identifier: CA2573136779

Gene: PIK3CA

Linked Data

• ClinVar Variation Id: 1498242
• ClinVar RCV Id: RCV002033906
• dbSNP Id: rs769124869
• gnomAD v4: 3-179218337-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179218337A>G , CM000665.2:g.179218337A>G	GRCh38
NC_000003.11:g.178936125A>G , CM000665.1:g.178936125A>G	GRCh37
NC_000003.10:g.180418819A>G	NCBI36
NG_012113.2:g.74815A>G , LRG_310:g.74815A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.1664+3A>G MANE Select	ENSP00000263967.3:n.1664+3A>G
ENST00000462255.2:n.126+3A>G
ENST00000643187.1:c.1664+3A>G	ENSP00000493507.1:n.1664+3A>G
ENST00000674534.1:n.1421A>G
ENST00000674622.1:c.167+3A>G	ENSP00000502417.1:n.167+3A>G
ENST00000675467.1:n.4471+3A>G
ENST00000675786.1:c.*231+3A>G	ENSP00000502323.1:n.*231+3A>G
ENST00000263967.3:c.1664+3A>G	ENSP00000263967.3:n.1664+3A>G
NM_006218.2:c.1664+3A>G , LRG_310t1:c.1664+3A>G	NP_006209.2:n.1664+3A>G
XM_006713658.2:c.1664+3A>G	XP_006713721.1:n.1664+3A>G
XM_011512894.1:c.1664+3A>G	XP_011511196.1:n.1664+3A>G
NM_006218.3:c.1664+3A>G	NP_006209.2:n.1664+3A>G
XM_006713658.4:c.1664+3A>G	XP_006713721.1:n.1664+3A>G
XM_011512894.2:c.1664+3A>G	XP_011511196.1:n.1664+3A>G
NM_006218.4:c.1664+3A>G MANE Select	NP_006209.2:n.1664+3A>G