Canonical Allele Identifier: CA891834938

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960942_87960944delinsTTT , CM000672.2:g.87960942_87960944delinsTTT	GRCh38
NC_000010.10:g.89720699_89720701delinsTTT , CM000672.1:g.89720699_89720701delinsTTT	GRCh37
NC_000010.9:g.89710679_89710681delinsTTT	NCBI36
NG_007466.2:g.102504_102506delinsTTT , LRG_311:g.102504_102506delinsTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.943_945delinsTTT	ENSP00000514759.2:p.Glu315Phe
ENST00000710265.1:c.850_852delinsTTT	ENSP00000518161.1:p.Glu284Phe
ENST00000472832.3:c.850_852delinsTTT	ENSP00000483066.2:p.Glu284Phe
ENST00000688158.2:n.1585_1587delinsTTT
ENST00000688922.2:c.*680_*682delinsTTT	ENSP00000508742.2:n.*680_*682delinsTTT
ENST00000700021.1:c.805_807delinsTTT	ENSP00000514757.1:p.Glu269Phe
ENST00000700022.1:c.*189_*191delinsTTT	ENSP00000514758.1:n.*189_*191delinsTTT
ENST00000700023.1:n.2008_2010delinsTTT
ENST00000700024.1:n.2242_2244delinsTTT
ENST00000700025.1:n.1619_1621delinsTTT
ENST00000700026.1:n.487_489delinsTTT
ENST00000700029.1:c.777_779delinsTTT
ENST00000706954.1:c.850_852delinsTTT	ENSP00000516674.1:p.Glu284Phe
ENST00000706955.1:c.*885_*887delinsTTT	ENSP00000516675.1:n.*885_*887delinsTTT
ENST00000686459.1:c.*436_*438delinsTTT	ENSP00000508909.1:n.*436_*438delinsTTT
ENST00000688158.1:c.*961_*963delinsTTT	ENSP00000509254.1:n.*961_*963delinsTTT
ENST00000688308.1:c.850_852delinsTTT	ENSP00000508752.1:p.Glu284Phe
ENST00000688922.1:c.771_773delinsTTT
ENST00000693560.1:c.1369_1371delinsTTT	ENSP00000509861.1:p.Glu457Phe
ENST00000371953.8:c.850_852delinsTTT MANE Select	ENSP00000361021.3:p.Glu284Phe
ENST00000371953.7:c.850_852delinsTTT	ENSP00000361021.3:p.Glu284Phe
ENST00000472832.2:c.277_279delinsTTT	ENSP00000483066.1:p.Glu93Phe
NM_000314.5:c.850_852delinsTTT	NP_000305.3:p.Glu284Phe
NM_000314.6:c.850_852delinsTTT	NP_000305.3:p.Glu284Phe
NM_001304717.2:c.1369_1371delinsTTT	NP_001291646.2:p.Glu457Phe
NM_001304718.1:c.259_261delinsTTT	NP_001291647.1:p.Glu87Phe
XM_006717926.2:c.805_807delinsTTT	XP_006717989.1:p.Glu269Phe
XM_011539981.1:c.850_852delinsTTT	XP_011538283.1:p.Glu284Phe
XM_011539982.1:c.754_756delinsTTT	XP_011538284.1:p.Glu252Phe
XR_945791.1:n.1420_1422delinsTTT
NM_000314.7:c.850_852delinsTTT	NP_000305.3:p.Glu284Phe
NM_001304717.5:c.1369_1371delinsTTT	NP_001291646.4:p.Glu457Phe
NM_001304718.2:c.259_261delinsTTT	NP_001291647.1:p.Glu87Phe
NM_000314.8:c.850_852delinsTTT MANE Select	NP_000305.3:p.Glu284Phe