Canonical Allele Identifier: CA136374

Gene: PIK3CA

Linked Data

• ClinVar Variation Id: 45467
• ClinVar RCV Id: RCV000038673 ; RCV001526503 ; RCV002254274 ; RCV003458194
• dbSNP Id: rs397517202
• COSMIC: COSM771 ; COSM1041519
• MyVariant Identifiers: chr3:g.178952018A>G (hg19) ; chr3:g.179234230A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179234230A>G , CM000665.2:g.179234230A>G	GRCh38
NC_000003.11:g.178952018A>G , CM000665.1:g.178952018A>G	GRCh37
NC_000003.10:g.180434712A>G	NCBI36
NG_012113.2:g.90708A>G , LRG_310:g.90708A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.3073A>G MANE Select	ENSP00000263967.3:p.Thr1025Ala
ENST00000462255.2:n.2096A>G
ENST00000643187.1:c.*153A>G	ENSP00000493507.1:n.*153A>G
ENST00000674534.1:n.3981A>G
ENST00000674622.1:c.1494A>G	ENSP00000502417.1:n.1494A>G
ENST00000675467.1:n.5880A>G
ENST00000675786.1:c.*1640A>G	ENSP00000502323.1:n.*1640A>G
ENST00000675796.1:n.2968A>G
ENST00000263967.3:c.3073A>G	ENSP00000263967.3:p.Thr1025Ala
NM_006218.2:c.3073A>G , LRG_310t1:c.3073A>G	NP_006209.2:p.Thr1025Ala
XM_006713658.2:c.3073A>G	XP_006713721.1:p.Thr1025Ala
XM_011512894.1:c.3073A>G	XP_011511196.1:p.Thr1025Ala
NM_006218.3:c.3073A>G	NP_006209.2:p.Thr1025Ala
XM_006713658.4:c.3073A>G	XP_006713721.1:p.Thr1025Ala
XM_011512894.2:c.3073A>G	XP_011511196.1:p.Thr1025Ala
NM_006218.4:c.3073A>G MANE Select	NP_006209.2:p.Thr1025Ala