Canonical Allele Identifier: CA891839872
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957963_87957964delinsTG , CM000672.2:g.87957963_87957964delinsTG GRCh38
NC_000010.10:g.89717720_89717721delinsTG , CM000672.1:g.89717720_89717721delinsTG GRCh37
NC_000010.9:g.89707700_89707701delinsTG NCBI36
NG_007466.2:g.99525_99526delinsTG , LRG_311:g.99525_99526delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.745_746delinsTG ENSP00000514759.2:p.Val249Trp
ENST00000710265.1:c.745_746delinsTG ENSP00000518161.1:p.Val249Trp
ENST00000472832.3:c.745_746delinsTG ENSP00000483066.2:p.Val249Trp
ENST00000688158.2:n.1480_1481delinsTG
ENST00000688922.2:c.*575_*576delinsTG ENSP00000508742.2:n.*575_*576delinsTG
ENST00000700021.1:c.700_701delinsTG ENSP00000514757.1:p.Val234Trp
ENST00000700022.1:c.*84_*85delinsTG ENSP00000514758.1:n.*84_*85delinsTG
ENST00000700023.1:n.1903_1904delinsTG
ENST00000700024.1:n.2137_2138delinsTG
ENST00000700025.1:n.1514_1515delinsTG
ENST00000700026.1:n.382_383delinsTG
ENST00000700029.1:c.579_580delinsTG
ENST00000706954.1:c.745_746delinsTG ENSP00000516674.1:p.Val249Trp
ENST00000706955.1:c.*780_*781delinsTG ENSP00000516675.1:n.*780_*781delinsTG
ENST00000686459.1:c.*331_*332delinsTG ENSP00000508909.1:n.*331_*332delinsTG
ENST00000688158.1:c.*856_*857delinsTG ENSP00000509254.1:n.*856_*857delinsTG
ENST00000688308.1:c.745_746delinsTG ENSP00000508752.1:p.Val249Trp
ENST00000688922.1:c.666_667delinsTG
ENST00000693560.1:c.1264_1265delinsTG ENSP00000509861.1:p.Val422Trp
ENST00000371953.8:c.745_746delinsTG MANE Select ENSP00000361021.3:p.Val249Trp
ENST00000371953.7:c.745_746delinsTG ENSP00000361021.3:p.Val249Trp
ENST00000472832.2:c.172_173delinsTG ENSP00000483066.1:p.Val58Trp
NM_000314.5:c.745_746delinsTG NP_000305.3:p.Val249Trp
NM_000314.6:c.745_746delinsTG NP_000305.3:p.Val249Trp
NM_001304717.2:c.1264_1265delinsTG NP_001291646.2:p.Val422Trp
NM_001304718.1:c.154_155delinsTG NP_001291647.1:p.Val52Trp
XM_006717926.2:c.700_701delinsTG XP_006717989.1:p.Val234Trp
XM_011539981.1:c.745_746delinsTG XP_011538283.1:p.Val249Trp
XM_011539982.1:c.649_650delinsTG XP_011538284.1:p.Val217Trp
XR_945791.1:n.1315_1316delinsTG
NM_000314.7:c.745_746delinsTG NP_000305.3:p.Val249Trp
NM_001304717.5:c.1264_1265delinsTG NP_001291646.4:p.Val422Trp
NM_001304718.2:c.154_155delinsTG NP_001291647.1:p.Val52Trp
NM_000314.8:c.745_746delinsTG MANE Select NP_000305.3:p.Val249Trp