Canonical Allele Identifier: CA2579926436
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965449_87965451delinsAGA , CM000672.2:g.87965449_87965451delinsAGA GRCh38
NC_000010.10:g.89725206_89725208delinsAGA , CM000672.1:g.89725206_89725208delinsAGA GRCh37
NC_000010.9:g.89715186_89715188delinsAGA NCBI36
NG_007466.2:g.107011_107013delinsAGA , LRG_311:g.107011_107013delinsAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1282_1284delinsAGA ENSP00000514759.2:p.His428Arg
ENST00000710265.1:c.*218_*220delinsAGA ENSP00000518161.1:n.*218_*220delinsAGA
ENST00000688158.2:n.1924_1926delinsAGA
ENST00000688922.2:c.*1019_*1021delinsAGA ENSP00000508742.2:n.*1019_*1021delinsAGA
ENST00000700021.1:c.1144_1146delinsAGA ENSP00000514757.1:p.His382Arg
ENST00000700022.1:c.*528_*530delinsAGA ENSP00000514758.1:n.*528_*530delinsAGA
ENST00000700023.1:n.2347_2349delinsAGA
ENST00000700024.1:n.2581_2583delinsAGA
ENST00000706954.1:c.1189_1191delinsAGA ENSP00000516674.1:p.His397Arg
ENST00000706955.1:c.*1224_*1226delinsAGA ENSP00000516675.1:n.*1224_*1226delinsAGA
ENST00000686459.1:c.*775_*777delinsAGA ENSP00000508909.1:n.*775_*777delinsAGA
ENST00000688158.1:c.*1300_*1302delinsAGA ENSP00000509254.1:n.*1300_*1302delinsAGA
ENST00000688308.1:c.1189_1191delinsAGA ENSP00000508752.1:p.His397Arg
ENST00000688922.1:c.1110_1112delinsAGA
ENST00000693560.1:c.1708_1710delinsAGA ENSP00000509861.1:p.His570Arg
ENST00000371953.8:c.1189_1191delinsAGA MANE Select ENSP00000361021.3:p.His397Arg
ENST00000371953.7:c.1189_1191delinsAGA ENSP00000361021.3:p.His397Arg
NM_000314.5:c.1189_1191delinsAGA NP_000305.3:p.His397Arg
NM_000314.6:c.1189_1191delinsAGA NP_000305.3:p.His397Arg
NM_001304717.2:c.1708_1710delinsAGA NP_001291646.2:p.His570Arg
NM_001304718.1:c.598_600delinsAGA NP_001291647.1:p.His200Arg
XM_006717926.2:c.1144_1146delinsAGA XP_006717989.1:p.His382Arg
XM_011539982.1:c.1093_1095delinsAGA XP_011538284.1:p.His365Arg
XR_945791.1:n.1759_1761delinsAGA
NM_000314.7:c.1189_1191delinsAGA NP_000305.3:p.His397Arg
NM_001304717.5:c.1708_1710delinsAGA NP_001291646.4:p.His570Arg
NM_001304718.2:c.598_600delinsAGA NP_001291647.1:p.His200Arg
NM_000314.8:c.1189_1191delinsAGA MANE Select NP_000305.3:p.His397Arg