Canonical Allele Identifier: CA891837738
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965386_87965388delinsTGG , CM000672.2:g.87965386_87965388delinsTGG GRCh38
NC_000010.10:g.89725143_89725145delinsTGG , CM000672.1:g.89725143_89725145delinsTGG GRCh37
NC_000010.9:g.89715123_89715125delinsTGG NCBI36
NG_007466.2:g.106948_106950delinsTGG , LRG_311:g.106948_106950delinsTGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1219_1221delinsTGG ENSP00000514759.2:p.His407Trp
ENST00000710265.1:c.*155_*157delinsTGG ENSP00000518161.1:n.*155_*157delinsTGG
ENST00000688158.2:n.1861_1863delinsTGG
ENST00000688922.2:c.*956_*958delinsTGG ENSP00000508742.2:n.*956_*958delinsTGG
ENST00000700021.1:c.1081_1083delinsTGG ENSP00000514757.1:p.His361Trp
ENST00000700022.1:c.*465_*467delinsTGG ENSP00000514758.1:n.*465_*467delinsTGG
ENST00000700023.1:n.2284_2286delinsTGG
ENST00000700024.1:n.2518_2520delinsTGG
ENST00000706954.1:c.1126_1128delinsTGG ENSP00000516674.1:p.His376Trp
ENST00000706955.1:c.*1161_*1163delinsTGG ENSP00000516675.1:n.*1161_*1163delinsTGG
ENST00000686459.1:c.*712_*714delinsTGG ENSP00000508909.1:n.*712_*714delinsTGG
ENST00000688158.1:c.*1237_*1239delinsTGG ENSP00000509254.1:n.*1237_*1239delinsTGG
ENST00000688308.1:c.1126_1128delinsTGG ENSP00000508752.1:p.His376Trp
ENST00000688922.1:c.1047_1049delinsTGG
ENST00000693560.1:c.1645_1647delinsTGG ENSP00000509861.1:p.His549Trp
ENST00000371953.8:c.1126_1128delinsTGG MANE Select ENSP00000361021.3:p.His376Trp
ENST00000371953.7:c.1126_1128delinsTGG ENSP00000361021.3:p.His376Trp
NM_000314.5:c.1126_1128delinsTGG NP_000305.3:p.His376Trp
NM_000314.6:c.1126_1128delinsTGG NP_000305.3:p.His376Trp
NM_001304717.2:c.1645_1647delinsTGG NP_001291646.2:p.His549Trp
NM_001304718.1:c.535_537delinsTGG NP_001291647.1:p.His179Trp
XM_006717926.2:c.1081_1083delinsTGG XP_006717989.1:p.His361Trp
XM_011539982.1:c.1030_1032delinsTGG XP_011538284.1:p.His344Trp
XR_945791.1:n.1696_1698delinsTGG
NM_000314.7:c.1126_1128delinsTGG NP_000305.3:p.His376Trp
NM_001304717.5:c.1645_1647delinsTGG NP_001291646.4:p.His549Trp
NM_001304718.2:c.535_537delinsTGG NP_001291647.1:p.His179Trp
NM_000314.8:c.1126_1128delinsTGG MANE Select NP_000305.3:p.His376Trp