Canonical Allele Identifier: CA2579926401
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965426_87965427delinsGA , CM000672.2:g.87965426_87965427delinsGA GRCh38
NC_000010.10:g.89725183_89725184delinsGA , CM000672.1:g.89725183_89725184delinsGA GRCh37
NC_000010.9:g.89715163_89715164delinsGA NCBI36
NG_007466.2:g.106988_106989delinsGA , LRG_311:g.106988_106989delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1259_1260delinsGA ENSP00000514759.2:p.Asn420Arg
ENST00000710265.1:c.*195_*196delinsGA ENSP00000518161.1:n.*195_*196delinsGA
ENST00000688158.2:n.1901_1902delinsGA
ENST00000688922.2:c.*996_*997delinsGA ENSP00000508742.2:n.*996_*997delinsGA
ENST00000700021.1:c.1121_1122delinsGA ENSP00000514757.1:p.Asn374Arg
ENST00000700022.1:c.*505_*506delinsGA ENSP00000514758.1:n.*505_*506delinsGA
ENST00000700023.1:n.2324_2325delinsGA
ENST00000700024.1:n.2558_2559delinsGA
ENST00000706954.1:c.1166_1167delinsGA ENSP00000516674.1:p.Asn389Arg
ENST00000706955.1:c.*1201_*1202delinsGA ENSP00000516675.1:n.*1201_*1202delinsGA
ENST00000686459.1:c.*752_*753delinsGA ENSP00000508909.1:n.*752_*753delinsGA
ENST00000688158.1:c.*1277_*1278delinsGA ENSP00000509254.1:n.*1277_*1278delinsGA
ENST00000688308.1:c.1166_1167delinsGA ENSP00000508752.1:p.Asn389Arg
ENST00000688922.1:c.1087_1088delinsGA
ENST00000693560.1:c.1685_1686delinsGA ENSP00000509861.1:p.Asn562Arg
ENST00000371953.8:c.1166_1167delinsGA MANE Select ENSP00000361021.3:p.Asn389Arg
ENST00000371953.7:c.1166_1167delinsGA ENSP00000361021.3:p.Asn389Arg
NM_000314.5:c.1166_1167delinsGA NP_000305.3:p.Asn389Arg
NM_000314.6:c.1166_1167delinsGA NP_000305.3:p.Asn389Arg
NM_001304717.2:c.1685_1686delinsGA NP_001291646.2:p.Asn562Arg
NM_001304718.1:c.575_576delinsGA NP_001291647.1:p.Asn192Arg
XM_006717926.2:c.1121_1122delinsGA XP_006717989.1:p.Asn374Arg
XM_011539982.1:c.1070_1071delinsGA XP_011538284.1:p.Asn357Arg
XR_945791.1:n.1736_1737delinsGA
NM_000314.7:c.1166_1167delinsGA NP_000305.3:p.Asn389Arg
NM_001304717.5:c.1685_1686delinsGA NP_001291646.4:p.Asn562Arg
NM_001304718.2:c.575_576delinsGA NP_001291647.1:p.Asn192Arg
NM_000314.8:c.1166_1167delinsGA MANE Select NP_000305.3:p.Asn389Arg