Canonical Allele Identifier: CA891837487
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965357_87965358delinsAT , CM000672.2:g.87965357_87965358delinsAT GRCh38
NC_000010.10:g.89725114_89725115delinsAT , CM000672.1:g.89725114_89725115delinsAT GRCh37
NC_000010.9:g.89715094_89715095delinsAT NCBI36
NG_007466.2:g.106919_106920delinsAT , LRG_311:g.106919_106920delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1190_1191delinsAT ENSP00000514759.2:p.Thr397Asn
ENST00000710265.1:c.*126_*127delinsAT ENSP00000518161.1:n.*126_*127delinsAT
ENST00000688158.2:n.1832_1833delinsAT
ENST00000688922.2:c.*927_*928delinsAT ENSP00000508742.2:n.*927_*928delinsAT
ENST00000700021.1:c.1052_1053delinsAT ENSP00000514757.1:p.Thr351Asn
ENST00000700022.1:c.*436_*437delinsAT ENSP00000514758.1:n.*436_*437delinsAT
ENST00000700023.1:n.2255_2256delinsAT
ENST00000700024.1:n.2489_2490delinsAT
ENST00000706954.1:c.1097_1098delinsAT ENSP00000516674.1:p.Thr366Asn
ENST00000706955.1:c.*1132_*1133delinsAT ENSP00000516675.1:n.*1132_*1133delinsAT
ENST00000686459.1:c.*683_*684delinsAT ENSP00000508909.1:n.*683_*684delinsAT
ENST00000688158.1:c.*1208_*1209delinsAT ENSP00000509254.1:n.*1208_*1209delinsAT
ENST00000688308.1:c.1097_1098delinsAT ENSP00000508752.1:p.Thr366Asn
ENST00000688922.1:c.1018_1019delinsAT
ENST00000693560.1:c.1616_1617delinsAT ENSP00000509861.1:p.Thr539Asn
ENST00000371953.8:c.1097_1098delinsAT MANE Select ENSP00000361021.3:p.Thr366Asn
ENST00000371953.7:c.1097_1098delinsAT ENSP00000361021.3:p.Thr366Asn
NM_000314.5:c.1097_1098delinsAT NP_000305.3:p.Thr366Asn
NM_000314.6:c.1097_1098delinsAT NP_000305.3:p.Thr366Asn
NM_001304717.2:c.1616_1617delinsAT NP_001291646.2:p.Thr539Asn
NM_001304718.1:c.506_507delinsAT NP_001291647.1:p.Thr169Asn
XM_006717926.2:c.1052_1053delinsAT XP_006717989.1:p.Thr351Asn
XM_011539982.1:c.1001_1002delinsAT XP_011538284.1:p.Thr334Asn
XR_945791.1:n.1667_1668delinsAT
NM_000314.7:c.1097_1098delinsAT NP_000305.3:p.Thr366Asn
NM_001304717.5:c.1616_1617delinsAT NP_001291646.4:p.Thr539Asn
NM_001304718.2:c.506_507delinsAT NP_001291647.1:p.Thr169Asn
NM_000314.8:c.1097_1098delinsAT MANE Select NP_000305.3:p.Thr366Asn