Canonical Allele Identifier: CA891841666
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965431_87965432delinsAA , CM000672.2:g.87965431_87965432delinsAA GRCh38
NC_000010.10:g.89725188_89725189delinsAA , CM000672.1:g.89725188_89725189delinsAA GRCh37
NC_000010.9:g.89715168_89715169delinsAA NCBI36
NG_007466.2:g.106993_106994delinsAA , LRG_311:g.106993_106994delinsAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1264_1265delinsAA ENSP00000514759.2:p.Pro422Asn
ENST00000710265.1:c.*200_*201delinsAA ENSP00000518161.1:n.*200_*201delinsAA
ENST00000688158.2:n.1906_1907delinsAA
ENST00000688922.2:c.*1001_*1002delinsAA ENSP00000508742.2:n.*1001_*1002delinsAA
ENST00000700021.1:c.1126_1127delinsAA ENSP00000514757.1:p.Pro376Asn
ENST00000700022.1:c.*510_*511delinsAA ENSP00000514758.1:n.*510_*511delinsAA
ENST00000700023.1:n.2329_2330delinsAA
ENST00000700024.1:n.2563_2564delinsAA
ENST00000706954.1:c.1171_1172delinsAA ENSP00000516674.1:p.Pro391Asn
ENST00000706955.1:c.*1206_*1207delinsAA ENSP00000516675.1:n.*1206_*1207delinsAA
ENST00000686459.1:c.*757_*758delinsAA ENSP00000508909.1:n.*757_*758delinsAA
ENST00000688158.1:c.*1282_*1283delinsAA ENSP00000509254.1:n.*1282_*1283delinsAA
ENST00000688308.1:c.1171_1172delinsAA ENSP00000508752.1:p.Pro391Asn
ENST00000688922.1:c.1092_1093delinsAA
ENST00000693560.1:c.1690_1691delinsAA ENSP00000509861.1:p.Pro564Asn
ENST00000371953.8:c.1171_1172delinsAA MANE Select ENSP00000361021.3:p.Pro391Asn
ENST00000371953.7:c.1171_1172delinsAA ENSP00000361021.3:p.Pro391Asn
NM_000314.5:c.1171_1172delinsAA NP_000305.3:p.Pro391Asn
NM_000314.6:c.1171_1172delinsAA NP_000305.3:p.Pro391Asn
NM_001304717.2:c.1690_1691delinsAA NP_001291646.2:p.Pro564Asn
NM_001304718.1:c.580_581delinsAA NP_001291647.1:p.Pro194Asn
XM_006717926.2:c.1126_1127delinsAA XP_006717989.1:p.Pro376Asn
XM_011539982.1:c.1075_1076delinsAA XP_011538284.1:p.Pro359Asn
XR_945791.1:n.1741_1742delinsAA
NM_000314.7:c.1171_1172delinsAA NP_000305.3:p.Pro391Asn
NM_001304717.5:c.1690_1691delinsAA NP_001291646.4:p.Pro564Asn
NM_001304718.2:c.580_581delinsAA NP_001291647.1:p.Pro194Asn
NM_000314.8:c.1171_1172delinsAA MANE Select NP_000305.3:p.Pro391Asn