Canonical Allele Identifier: CA437315930

Gene: PIK3CA

Linked Data

• COSMIC: COSM166341
• MyVariant Identifiers: chr3:g.178921444del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179203656del , CM000665.2:g.179203656del	GRCh38
NC_000003.11:g.178921444del , CM000665.1:g.178921444del	GRCh37
NC_000003.10:g.180404138del	NCBI36
NG_012113.2:g.60134del , LRG_310:g.60134del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.926del MANE Select	ENSP00000263967.3:p.Arg309AsnfsTer10
ENST00000643187.1:c.926del	ENSP00000493507.1:p.Arg309AsnfsTer10
ENST00000674534.1:n.680del
ENST00000675467.1:n.3733del
ENST00000675786.1:c.926del	ENSP00000502323.1:p.Arg309AsnfsTer10
ENST00000263967.3:c.926del	ENSP00000263967.3:p.Arg309AsnfsTer10
NM_006218.2:c.926del , LRG_310t1:c.926del	NP_006209.2:p.Arg309AsnfsTer10
XM_006713658.2:c.926del	XP_006713721.1:p.Arg309AsnfsTer10
XM_011512894.1:c.926del	XP_011511196.1:p.Arg309AsnfsTer10
NM_006218.3:c.926del	NP_006209.2:p.Arg309AsnfsTer10
XM_006713658.4:c.926del	XP_006713721.1:p.Arg309AsnfsTer10
XM_011512894.2:c.926del	XP_011511196.1:p.Arg309AsnfsTer10
NM_006218.4:c.926del MANE Select	NP_006209.2:p.Arg309AsnfsTer10