Canonical Allele Identifier: CA2577963159

Gene: PIK3CA

Linked Data

• gnomAD v4: 3-179219620-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179219622del , CM000665.2:g.179219622del	GRCh38
NC_000003.11:g.178937410del , CM000665.1:g.178937410del	GRCh37
NC_000003.10:g.180420104del	NCBI36
NG_012113.2:g.76100del , LRG_310:g.76100del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.1798del MANE Select	ENSP00000263967.3:p.Glu600AsnfsTer24
ENST00000462255.2:n.260del
ENST00000643187.1:c.1798del	ENSP00000493507.1:p.Glu600AsnfsTer24
ENST00000674534.1:n.2706del
ENST00000674622.1:c.219del	ENSP00000502417.1:n.219del
ENST00000675467.1:n.4605del
ENST00000675786.1:c.*365del	ENSP00000502323.1:n.*365del
ENST00000263967.3:c.1798del	ENSP00000263967.3:p.Glu600AsnfsTer24
ENST00000462255.1:n.72del
NM_006218.2:c.1798del , LRG_310t1:c.1798del	NP_006209.2:p.Glu600AsnfsTer24
XM_006713658.2:c.1798del	XP_006713721.1:p.Glu600AsnfsTer24
XM_011512894.1:c.1798del	XP_011511196.1:p.Glu600AsnfsTer24
NM_006218.3:c.1798del	NP_006209.2:p.Glu600AsnfsTer24
XM_006713658.4:c.1798del	XP_006713721.1:p.Glu600AsnfsTer24
XM_011512894.2:c.1798del	XP_011511196.1:p.Glu600AsnfsTer24
NM_006218.4:c.1798del MANE Select	NP_006209.2:p.Glu600AsnfsTer24