Canonical Allele Identifier: CA1423676455

Gene: PIK3CA

Linked Data

• ClinVar Variation Id: 1047316
• ClinVar RCV Id: RCV001352011
• dbSNP Id: rs1725283257

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179234296_179234297delinsAT , CM000665.2:g.179234296_179234297delinsAT	GRCh38
NC_000003.11:g.178952084_178952085delinsAT , CM000665.1:g.178952084_178952085delinsAT	GRCh37
NC_000003.10:g.180434778_180434779delinsAT	NCBI36
NG_012113.2:g.90774_90775delinsAT , LRG_310:g.90774_90775delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000263967.4:c.3139_3140delinsAT MANE Select	ENSP00000263967.3:p.His1047Ile
ENST00000462255.2:n.2162_2163delinsAT
ENST00000643187.1:c.*219_*220delinsAT	ENSP00000493507.1:n.*219_*220delinsAT
ENST00000674534.1:n.4047_4048delinsAT
ENST00000674622.1:c.1560_1561delinsAT	ENSP00000502417.1:n.1560_1561delinsAT
ENST00000675467.1:n.5946_5947delinsAT
ENST00000675786.1:c.*1706_*1707delinsAT	ENSP00000502323.1:n.*1706_*1707delinsAT
ENST00000675796.1:n.3034_3035delinsAT
ENST00000263967.3:c.3139_3140delinsAT	ENSP00000263967.3:p.His1047Ile
NM_006218.2:c.3139_3140delinsAT , LRG_310t1:c.3139_3140delinsAT	NP_006209.2:p.His1047Ile
XM_006713658.2:c.3139_3140delinsAT	XP_006713721.1:p.His1047Ile
XM_011512894.1:c.3139_3140delinsAT	XP_011511196.1:p.His1047Ile
NM_006218.3:c.3139_3140delinsAT	NP_006209.2:p.His1047Ile
XM_006713658.4:c.3139_3140delinsAT	XP_006713721.1:p.His1047Ile
XM_011512894.2:c.3139_3140delinsAT	XP_011511196.1:p.His1047Ile
NM_006218.4:c.3139_3140delinsAT MANE Select	NP_006209.2:p.His1047Ile