Canonical Allele Identifier: CA2668619710

Gene: PIK3CA

Linked Data

• gnomAD v4: 3-179199035-CGTAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179199038_179199041del , CM000665.2:g.179199038_179199041del	GRCh38
NC_000003.11:g.178916826_178916829del , CM000665.1:g.178916826_178916829del	GRCh37
NC_000003.10:g.180399520_180399523del	NCBI36
NG_012113.2:g.55516_55519del , LRG_310:g.55516_55519del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.213_216del MANE Select	ENSP00000263967.3:p.Ser72LeufsTer27
ENST00000643187.1:c.213_216del	ENSP00000493507.1:p.Ser72LeufsTer27
ENST00000675467.1:n.3020_3023del
ENST00000675786.1:c.213_216del	ENSP00000502323.1:p.Ser72LeufsTer27
ENST00000263967.3:c.213_216del	ENSP00000263967.3:p.Ser72LeufsTer27
ENST00000468036.1:c.213_216del	ENSP00000417479.1:p.Ser72LeufsTer27
NM_006218.2:c.213_216del , LRG_310t1:c.213_216del	NP_006209.2:p.Ser72LeufsTer27
XM_006713658.2:c.213_216del	XP_006713721.1:p.Ser72LeufsTer27
XM_011512894.1:c.213_216del	XP_011511196.1:p.Ser72LeufsTer27
NM_006218.3:c.213_216del	NP_006209.2:p.Ser72LeufsTer27
XM_006713658.4:c.213_216del	XP_006713721.1:p.Ser72LeufsTer27
XM_011512894.2:c.213_216del	XP_011511196.1:p.Ser72LeufsTer27
NM_006218.4:c.213_216del MANE Select	NP_006209.2:p.Ser72LeufsTer27