Canonical Allele Identifier: CA658796394

Gene: PIK3CA

Linked Data

• ClinVar Variation Id: 526633
• ClinVar RCV Id: RCV000631210
• dbSNP Id: rs1553821123
• MyVariant Identifiers: chr3:g.178921522_178921523del (hg19) ; chr3:g.179203734_179203735del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179203734_179203735del , CM000665.2:g.179203734_179203735del	GRCh38
NC_000003.11:g.178921522_178921523del , CM000665.1:g.178921522_178921523del	GRCh37
NC_000003.10:g.180404216_180404217del	NCBI36
NG_012113.2:g.60212_60213del , LRG_310:g.60212_60213del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.1004_1005del MANE Select	ENSP00000263967.3:p.Arg335AsnfsTer17
ENST00000643187.1:c.1004_1005del	ENSP00000493507.1:p.Arg335AsnfsTer17
ENST00000674534.1:n.758_759del
ENST00000675467.1:n.3811_3812del
ENST00000675786.1:c.1004_1005del	ENSP00000502323.1:p.Arg335AsnfsTer17
ENST00000263967.3:c.1004_1005del	ENSP00000263967.3:p.Arg335AsnfsTer17
NM_006218.2:c.1004_1005del , LRG_310t1:c.1004_1005del	NP_006209.2:p.Arg335AsnfsTer17
XM_006713658.2:c.1004_1005del	XP_006713721.1:p.Arg335AsnfsTer17
XM_011512894.1:c.1004_1005del	XP_011511196.1:p.Arg335AsnfsTer17
NM_006218.3:c.1004_1005del	NP_006209.2:p.Arg335AsnfsTer17
XM_006713658.4:c.1004_1005del	XP_006713721.1:p.Arg335AsnfsTer17
XM_011512894.2:c.1004_1005del	XP_011511196.1:p.Arg335AsnfsTer17
NM_006218.4:c.1004_1005del MANE Select	NP_006209.2:p.Arg335AsnfsTer17