Canonical Allele Identifier: CA355280658

Gene: PIK3CA

Linked Data

• ClinVar Variation Id: 2031542
• ClinVar RCV Id: RCV002898866
• gnomAD v4: 3-179203682-A-G
• MyVariant Identifiers: chr3:g.178921470A>G (hg19) ; chr3:g.179203682A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179203682A>G , CM000665.2:g.179203682A>G	GRCh38
NC_000003.11:g.178921470A>G , CM000665.1:g.178921470A>G	GRCh37
NC_000003.10:g.180404164A>G	NCBI36
NG_012113.2:g.60160A>G , LRG_310:g.60160A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.952A>G MANE Select	ENSP00000263967.3:p.Met318Val
ENST00000643187.1:c.952A>G	ENSP00000493507.1:p.Met318Val
ENST00000674534.1:n.706A>G
ENST00000675467.1:n.3759A>G
ENST00000675786.1:c.952A>G	ENSP00000502323.1:p.Met318Val
ENST00000263967.3:c.952A>G	ENSP00000263967.3:p.Met318Val
NM_006218.2:c.952A>G , LRG_310t1:c.952A>G	NP_006209.2:p.Met318Val
XM_006713658.2:c.952A>G	XP_006713721.1:p.Met318Val
XM_011512894.1:c.952A>G	XP_011511196.1:p.Met318Val
NM_006218.3:c.952A>G	NP_006209.2:p.Met318Val
XM_006713658.4:c.952A>G	XP_006713721.1:p.Met318Val
XM_011512894.2:c.952A>G	XP_011511196.1:p.Met318Val
NM_006218.4:c.952A>G MANE Select	NP_006209.2:p.Met318Val