Canonical Allele Identifier: CA891837733
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965386_87965388delinsAGA , CM000672.2:g.87965386_87965388delinsAGA GRCh38
NC_000010.10:g.89725143_89725145delinsAGA , CM000672.1:g.89725143_89725145delinsAGA GRCh37
NC_000010.9:g.89715123_89715125delinsAGA NCBI36
NG_007466.2:g.106948_106950delinsAGA , LRG_311:g.106948_106950delinsAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1219_1221delinsAGA ENSP00000514759.2:p.His407Arg
ENST00000710265.1:c.*155_*157delinsAGA ENSP00000518161.1:n.*155_*157delinsAGA
ENST00000688158.2:n.1861_1863delinsAGA
ENST00000688922.2:c.*956_*958delinsAGA ENSP00000508742.2:n.*956_*958delinsAGA
ENST00000700021.1:c.1081_1083delinsAGA ENSP00000514757.1:p.His361Arg
ENST00000700022.1:c.*465_*467delinsAGA ENSP00000514758.1:n.*465_*467delinsAGA
ENST00000700023.1:n.2284_2286delinsAGA
ENST00000700024.1:n.2518_2520delinsAGA
ENST00000706954.1:c.1126_1128delinsAGA ENSP00000516674.1:p.His376Arg
ENST00000706955.1:c.*1161_*1163delinsAGA ENSP00000516675.1:n.*1161_*1163delinsAGA
ENST00000686459.1:c.*712_*714delinsAGA ENSP00000508909.1:n.*712_*714delinsAGA
ENST00000688158.1:c.*1237_*1239delinsAGA ENSP00000509254.1:n.*1237_*1239delinsAGA
ENST00000688308.1:c.1126_1128delinsAGA ENSP00000508752.1:p.His376Arg
ENST00000688922.1:c.1047_1049delinsAGA
ENST00000693560.1:c.1645_1647delinsAGA ENSP00000509861.1:p.His549Arg
ENST00000371953.8:c.1126_1128delinsAGA MANE Select ENSP00000361021.3:p.His376Arg
ENST00000371953.7:c.1126_1128delinsAGA ENSP00000361021.3:p.His376Arg
NM_000314.5:c.1126_1128delinsAGA NP_000305.3:p.His376Arg
NM_000314.6:c.1126_1128delinsAGA NP_000305.3:p.His376Arg
NM_001304717.2:c.1645_1647delinsAGA NP_001291646.2:p.His549Arg
NM_001304718.1:c.535_537delinsAGA NP_001291647.1:p.His179Arg
XM_006717926.2:c.1081_1083delinsAGA XP_006717989.1:p.His361Arg
XM_011539982.1:c.1030_1032delinsAGA XP_011538284.1:p.His344Arg
XR_945791.1:n.1696_1698delinsAGA
NM_000314.7:c.1126_1128delinsAGA NP_000305.3:p.His376Arg
NM_001304717.5:c.1645_1647delinsAGA NP_001291646.4:p.His549Arg
NM_001304718.2:c.535_537delinsAGA NP_001291647.1:p.His179Arg
NM_000314.8:c.1126_1128delinsAGA MANE Select NP_000305.3:p.His376Arg