Canonical Allele Identifier: CA437032934

Gene: PIK3CA

Linked Data

• COSMIC: COSM1651761
• MyVariant Identifiers: chr3:g.178936118del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179218330del , CM000665.2:g.179218330del	GRCh38
NC_000003.11:g.178936118del , CM000665.1:g.178936118del	GRCh37
NC_000003.10:g.180418812del	NCBI36
NG_012113.2:g.74808del , LRG_310:g.74808del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.1660del MANE Select	ENSP00000263967.3:p.His554ThrfsTer6
ENST00000462255.2:n.122del
ENST00000643187.1:c.1660del	ENSP00000493507.1:p.His554ThrfsTer6
ENST00000674534.1:n.1414del
ENST00000674622.1:c.163del	ENSP00000502417.1:p.His55ThrfsTer15
ENST00000675467.1:n.4467del
ENST00000675786.1:c.*227del	ENSP00000502323.1:n.*227del
ENST00000263967.3:c.1660del	ENSP00000263967.3:p.His554ThrfsTer6
NM_006218.2:c.1660del , LRG_310t1:c.1660del	NP_006209.2:p.His554ThrfsTer6
XM_006713658.2:c.1660del	XP_006713721.1:p.His554ThrfsTer6
XM_011512894.1:c.1660del	XP_011511196.1:p.His554ThrfsTer6
NM_006218.3:c.1660del	NP_006209.2:p.His554ThrfsTer6
XM_006713658.4:c.1660del	XP_006713721.1:p.His554ThrfsTer6
XM_011512894.2:c.1660del	XP_011511196.1:p.His554ThrfsTer6
NM_006218.4:c.1660del MANE Select	NP_006209.2:p.His554ThrfsTer6