Canonical Allele Identifier: CA891837914
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965407_87965409delinsTGG , CM000672.2:g.87965407_87965409delinsTGG GRCh38
NC_000010.10:g.89725164_89725166delinsTGG , CM000672.1:g.89725164_89725166delinsTGG GRCh37
NC_000010.9:g.89715144_89715146delinsTGG NCBI36
NG_007466.2:g.106969_106971delinsTGG , LRG_311:g.106969_106971delinsTGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1240_1242delinsTGG ENSP00000514759.2:p.Thr414Trp
ENST00000710265.1:c.*176_*178delinsTGG ENSP00000518161.1:n.*176_*178delinsTGG
ENST00000688158.2:n.1882_1884delinsTGG
ENST00000688922.2:c.*977_*979delinsTGG ENSP00000508742.2:n.*977_*979delinsTGG
ENST00000700021.1:c.1102_1104delinsTGG ENSP00000514757.1:p.Thr368Trp
ENST00000700022.1:c.*486_*488delinsTGG ENSP00000514758.1:n.*486_*488delinsTGG
ENST00000700023.1:n.2305_2307delinsTGG
ENST00000700024.1:n.2539_2541delinsTGG
ENST00000706954.1:c.1147_1149delinsTGG ENSP00000516674.1:p.Thr383Trp
ENST00000706955.1:c.*1182_*1184delinsTGG ENSP00000516675.1:n.*1182_*1184delinsTGG
ENST00000686459.1:c.*733_*735delinsTGG ENSP00000508909.1:n.*733_*735delinsTGG
ENST00000688158.1:c.*1258_*1260delinsTGG ENSP00000509254.1:n.*1258_*1260delinsTGG
ENST00000688308.1:c.1147_1149delinsTGG ENSP00000508752.1:p.Thr383Trp
ENST00000688922.1:c.1068_1070delinsTGG
ENST00000693560.1:c.1666_1668delinsTGG ENSP00000509861.1:p.Thr556Trp
ENST00000371953.8:c.1147_1149delinsTGG MANE Select ENSP00000361021.3:p.Thr383Trp
ENST00000371953.7:c.1147_1149delinsTGG ENSP00000361021.3:p.Thr383Trp
NM_000314.5:c.1147_1149delinsTGG NP_000305.3:p.Thr383Trp
NM_000314.6:c.1147_1149delinsTGG NP_000305.3:p.Thr383Trp
NM_001304717.2:c.1666_1668delinsTGG NP_001291646.2:p.Thr556Trp
NM_001304718.1:c.556_558delinsTGG NP_001291647.1:p.Thr186Trp
XM_006717926.2:c.1102_1104delinsTGG XP_006717989.1:p.Thr368Trp
XM_011539982.1:c.1051_1053delinsTGG XP_011538284.1:p.Thr351Trp
XR_945791.1:n.1717_1719delinsTGG
NM_000314.7:c.1147_1149delinsTGG NP_000305.3:p.Thr383Trp
NM_001304717.5:c.1666_1668delinsTGG NP_001291646.4:p.Thr556Trp
NM_001304718.2:c.556_558delinsTGG NP_001291647.1:p.Thr186Trp
NM_000314.8:c.1147_1149delinsTGG MANE Select NP_000305.3:p.Thr383Trp