Canonical Allele Identifier: CA547860610

Gene: PIK3CA

Linked Data

• dbSNP Id: rs1204182885
• gnomAD v2: 3-178936226-ATAAAG-A
• gnomAD v3: 3-179218438-ATAAAG-A
• gnomAD v4: 3-179218438-ATAAAG-A
• MyVariant Identifiers: chr3:g.178936227_178936231del (hg19) ; chr3:g.179218439_179218443del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179218439_179218443del , CM000665.2:g.179218439_179218443del	GRCh38
NC_000003.11:g.178936227_178936231del , CM000665.1:g.178936227_178936231del	GRCh37
NC_000003.10:g.180418921_180418925del	NCBI36
NG_012113.2:g.74917_74921del , LRG_310:g.74917_74921del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.1664+105_1664+109del MANE Select	ENSP00000263967.3:n.1664+105_1664+109del
ENST00000462255.2:n.126+105_126+109del
ENST00000643187.1:c.1664+105_1664+109del	ENSP00000493507.1:n.1664+105_1664+109del
ENST00000674534.1:n.1523_1527del
ENST00000674622.1:c.167+105_167+109del	ENSP00000502417.1:n.167+105_167+109del
ENST00000675467.1:n.4471+105_4471+109del
ENST00000675786.1:c.*231+105_*231+109del	ENSP00000502323.1:n.*231+105_*231+109del
ENST00000263967.3:c.1664+105_1664+109del	ENSP00000263967.3:n.1664+105_1664+109del
NM_006218.2:c.1664+105_1664+109del , LRG_310t1:c.1664+105_1664+109del	NP_006209.2:n.1664+105_1664+109del
XM_006713658.2:c.1664+105_1664+109del	XP_006713721.1:n.1664+105_1664+109del
XM_011512894.1:c.1664+105_1664+109del	XP_011511196.1:n.1664+105_1664+109del
NM_006218.3:c.1664+105_1664+109del	NP_006209.2:n.1664+105_1664+109del
XM_006713658.4:c.1664+105_1664+109del	XP_006713721.1:n.1664+105_1664+109del
XM_011512894.2:c.1664+105_1664+109del	XP_011511196.1:n.1664+105_1664+109del
NM_006218.4:c.1664+105_1664+109del MANE Select	NP_006209.2:n.1664+105_1664+109del