Canonical Allele Identifier: CA891834936

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960942_87960943delinsTG , CM000672.2:g.87960942_87960943delinsTG	GRCh38
NC_000010.10:g.89720699_89720700delinsTG , CM000672.1:g.89720699_89720700delinsTG	GRCh37
NC_000010.9:g.89710679_89710680delinsTG	NCBI36
NG_007466.2:g.102504_102505delinsTG , LRG_311:g.102504_102505delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.943_944delinsTG	ENSP00000514759.2:p.Glu315Trp
ENST00000710265.1:c.850_851delinsTG	ENSP00000518161.1:p.Glu284Trp
ENST00000472832.3:c.850_851delinsTG	ENSP00000483066.2:p.Glu284Trp
ENST00000688158.2:n.1585_1586delinsTG
ENST00000688922.2:c.*680_*681delinsTG	ENSP00000508742.2:n.*680_*681delinsTG
ENST00000700021.1:c.805_806delinsTG	ENSP00000514757.1:p.Glu269Trp
ENST00000700022.1:c.*189_*190delinsTG	ENSP00000514758.1:n.*189_*190delinsTG
ENST00000700023.1:n.2008_2009delinsTG
ENST00000700024.1:n.2242_2243delinsTG
ENST00000700025.1:n.1619_1620delinsTG
ENST00000700026.1:n.487_488delinsTG
ENST00000700029.1:c.777_778delinsTG
ENST00000706954.1:c.850_851delinsTG	ENSP00000516674.1:p.Glu284Trp
ENST00000706955.1:c.*885_*886delinsTG	ENSP00000516675.1:n.*885_*886delinsTG
ENST00000686459.1:c.*436_*437delinsTG	ENSP00000508909.1:n.*436_*437delinsTG
ENST00000688158.1:c.*961_*962delinsTG	ENSP00000509254.1:n.*961_*962delinsTG
ENST00000688308.1:c.850_851delinsTG	ENSP00000508752.1:p.Glu284Trp
ENST00000688922.1:c.771_772delinsTG
ENST00000693560.1:c.1369_1370delinsTG	ENSP00000509861.1:p.Glu457Trp
ENST00000371953.8:c.850_851delinsTG MANE Select	ENSP00000361021.3:p.Glu284Trp
ENST00000371953.7:c.850_851delinsTG	ENSP00000361021.3:p.Glu284Trp
ENST00000472832.2:c.277_278delinsTG	ENSP00000483066.1:p.Glu93Trp
NM_000314.5:c.850_851delinsTG	NP_000305.3:p.Glu284Trp
NM_000314.6:c.850_851delinsTG	NP_000305.3:p.Glu284Trp
NM_001304717.2:c.1369_1370delinsTG	NP_001291646.2:p.Glu457Trp
NM_001304718.1:c.259_260delinsTG	NP_001291647.1:p.Glu87Trp
XM_006717926.2:c.805_806delinsTG	XP_006717989.1:p.Glu269Trp
XM_011539981.1:c.850_851delinsTG	XP_011538283.1:p.Glu284Trp
XM_011539982.1:c.754_755delinsTG	XP_011538284.1:p.Glu252Trp
XR_945791.1:n.1420_1421delinsTG
NM_000314.7:c.850_851delinsTG	NP_000305.3:p.Glu284Trp
NM_001304717.5:c.1369_1370delinsTG	NP_001291646.4:p.Glu457Trp
NM_001304718.2:c.259_260delinsTG	NP_001291647.1:p.Glu87Trp
NM_000314.8:c.850_851delinsTG MANE Select	NP_000305.3:p.Glu284Trp