Canonical Allele Identifier: CA658796393

Gene: PIK3CA

Linked Data

• ClinVar Variation Id: 498669
• ClinVar RCV Id: RCV000592860
• dbSNP Id: rs1553820381
• MyVariant Identifiers: chr3:g.178916924_178916935del (hg19) ; chr3:g.179199136_179199147del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179199136_179199147del , CM000665.2:g.179199136_179199147del	GRCh38
NC_000003.11:g.178916924_178916935del , CM000665.1:g.178916924_178916935del	GRCh37
NC_000003.10:g.180399618_180399629del	NCBI36
NG_012113.2:g.55614_55625del , LRG_310:g.55614_55625del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.311_322del MANE Select	ENSP00000263967.3:p.Pro104_Asn107del
ENST00000643187.1:c.311_322del	ENSP00000493507.1:p.Pro104_Asn107del
ENST00000675467.1:n.3118_3129del
ENST00000675786.1:c.311_322del	ENSP00000502323.1:p.Pro104_Asn107del
ENST00000263967.3:c.311_322del	ENSP00000263967.3:p.Pro104_Asn107del
ENST00000468036.1:c.311_322del	ENSP00000417479.1:p.Pro104_Asn107del
NM_006218.2:c.311_322del , LRG_310t1:c.311_322del	NP_006209.2:p.Pro104_Asn107del
XM_006713658.2:c.311_322del	XP_006713721.1:p.Pro104_Asn107del
XM_011512894.1:c.311_322del	XP_011511196.1:p.Pro104_Asn107del
NM_006218.3:c.311_322del	NP_006209.2:p.Pro104_Asn107del
XM_006713658.4:c.311_322del	XP_006713721.1:p.Pro104_Asn107del
XM_011512894.2:c.311_322del	XP_011511196.1:p.Pro104_Asn107del
NM_006218.4:c.311_322del MANE Select	NP_006209.2:p.Pro104_Asn107del