Canonical Allele Identifier: CA136368

Gene: PIK3CA

Linked Data

• ClinVar Variation Id: 45465
• ClinVar RCV Id: RCV000038670
• dbSNP Id: rs397517200
• MyVariant Identifiers: chr3:g.178928081_178928095del (hg19) ; chr3:g.179210293_179210307del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179210293_179210307del , CM000665.2:g.179210293_179210307del	GRCh38
NC_000003.11:g.178928081_178928095del , CM000665.1:g.178928081_178928095del	GRCh37
NC_000003.10:g.180410775_180410789del	NCBI36
NG_012113.2:g.66771_66785del , LRG_310:g.66771_66785del

Transcript Alleles

HGVS	Amino-acid change
ENST00000263967.4:c.1359_1373del MANE Select	ENSP00000263967.3:p.Glu453_Pro458delinsAs...
ENST00000643187.1:c.1359_1373del	ENSP00000493507.1:p.Glu453_Pro458delinsAs...
ENST00000674534.1:n.1113_1127del
ENST00000675467.1:n.4166_4180del
ENST00000675786.1:c.1359_1373del	ENSP00000502323.1:p.Glu453_Pro458delinsAs...
ENST00000263967.3:c.1359_1373del	ENSP00000263967.3:p.Glu453_Pro458delinsAs...
NM_006218.2:c.1359_1373del , LRG_310t1:c.1359_1373del	NP_006209.2:p.Glu453_Pro458delinsAsp
XM_006713658.2:c.1359_1373del	XP_006713721.1:p.Glu453_Pro458delinsAsp
XM_011512894.1:c.1359_1373del	XP_011511196.1:p.Glu453_Pro458delinsAsp
NM_006218.3:c.1359_1373del	NP_006209.2:p.Glu453_Pro458delinsAsp
XM_006713658.4:c.1359_1373del	XP_006713721.1:p.Glu453_Pro458delinsAsp
XM_011512894.2:c.1359_1373del	XP_011511196.1:p.Glu453_Pro458delinsAsp
NM_006218.4:c.1359_1373del MANE Select	NP_006209.2:p.Glu453_Pro458delinsAsp