Canonical Allele Identifier: CA891835560

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87894102_87894104delinsTAT , CM000672.2:g.87894102_87894104delinsTAT	GRCh38
NC_000010.10:g.89653859_89653861delinsTAT , CM000672.1:g.89653859_89653861delinsTAT	GRCh37
NC_000010.9:g.89643839_89643841delinsTAT	NCBI36
NG_007466.2:g.35664_35666delinsTAT , LRG_311:g.35664_35666delinsTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.157_159delinsTAT	ENSP00000514759.2:p.Val53Tyr
ENST00000710265.1:c.157_159delinsTAT	ENSP00000518161.1:p.Val53Tyr
ENST00000472832.3:c.157_159delinsTAT	ENSP00000483066.2:p.Val53Tyr
ENST00000688158.2:n.899+13664_899+13666delinsTAT
ENST00000688922.2:c.157_159delinsTAT	ENSP00000508742.2:p.Val53Tyr
ENST00000700021.1:c.157_159delinsTAT	ENSP00000514757.1:p.Val53Tyr
ENST00000700022.1:c.157_159delinsTAT	ENSP00000514758.1:p.Val53Tyr
ENST00000706954.1:c.157_159delinsTAT	ENSP00000516674.1:p.Val53Tyr
ENST00000706955.1:c.*192_*194delinsTAT	ENSP00000516675.1:n.*192_*194delinsTAT
ENST00000686459.1:c.157_159delinsTAT	ENSP00000508909.1:p.Val53Tyr
ENST00000688158.1:c.*275+13664_*275+13666delinsTAT	ENSP00000509254.1:n.*275+13664_*275+13666delinsTAT
ENST00000688308.1:c.157_159delinsTAT	ENSP00000508752.1:p.Val53Tyr
ENST00000688922.1:c.26_28delinsTAT
ENST00000693560.1:c.676_678delinsTAT	ENSP00000509861.1:p.Val226Tyr
ENST00000371953.8:c.157_159delinsTAT MANE Select	ENSP00000361021.3:p.Val53Tyr
ENST00000371953.7:c.157_159delinsTAT	ENSP00000361021.3:p.Val53Tyr
ENST00000462694.1:n.159_161delinsTAT
ENST00000610634.1:c.55_57delinsTAT	ENSP00000477517.1:p.Val19Tyr
NM_000314.5:c.157_159delinsTAT	NP_000305.3:p.Val53Tyr
NM_000314.6:c.157_159delinsTAT	NP_000305.3:p.Val53Tyr
NM_001304717.2:c.676_678delinsTAT	NP_001291646.2:p.Val226Tyr
NM_001304718.1:c.-549_-547delinsTAT	NP_001291647.1:n.-549_-547delinsTAT
XM_006717926.2:c.157_159delinsTAT	XP_006717989.1:p.Val53Tyr
XM_011539981.1:c.157_159delinsTAT	XP_011538283.1:p.Val53Tyr
XM_011539982.1:c.68+13664_68+13666delinsTAT	XP_011538284.1:n.68+13664_68+13666delinsTAT
XR_945789.1:n.869_871delinsTAT
XR_945790.1:n.869_871delinsTAT
XR_945791.1:n.869_871delinsTAT
NM_000314.7:c.157_159delinsTAT	NP_000305.3:p.Val53Tyr
NM_001304717.5:c.676_678delinsTAT	NP_001291646.4:p.Val226Tyr
NM_001304718.2:c.-549_-547delinsTAT	NP_001291647.1:n.-549_-547delinsTAT
NM_000314.8:c.157_159delinsTAT MANE Select	NP_000305.3:p.Val53Tyr