Canonical Allele Identifier: CA891837558
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965365_87965366delinsAC , CM000672.2:g.87965365_87965366delinsAC GRCh38
NC_000010.10:g.89725122_89725123delinsAC , CM000672.1:g.89725122_89725123delinsAC GRCh37
NC_000010.9:g.89715102_89715103delinsAC NCBI36
NG_007466.2:g.106927_106928delinsAC , LRG_311:g.106927_106928delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1198_1199delinsAC ENSP00000514759.2:p.Val400Thr
ENST00000710265.1:c.*134_*135delinsAC ENSP00000518161.1:n.*134_*135delinsAC
ENST00000688158.2:n.1840_1841delinsAC
ENST00000688922.2:c.*935_*936delinsAC ENSP00000508742.2:n.*935_*936delinsAC
ENST00000700021.1:c.1060_1061delinsAC ENSP00000514757.1:p.Val354Thr
ENST00000700022.1:c.*444_*445delinsAC ENSP00000514758.1:n.*444_*445delinsAC
ENST00000700023.1:n.2263_2264delinsAC
ENST00000700024.1:n.2497_2498delinsAC
ENST00000706954.1:c.1105_1106delinsAC ENSP00000516674.1:p.Val369Thr
ENST00000706955.1:c.*1140_*1141delinsAC ENSP00000516675.1:n.*1140_*1141delinsAC
ENST00000686459.1:c.*691_*692delinsAC ENSP00000508909.1:n.*691_*692delinsAC
ENST00000688158.1:c.*1216_*1217delinsAC ENSP00000509254.1:n.*1216_*1217delinsAC
ENST00000688308.1:c.1105_1106delinsAC ENSP00000508752.1:p.Val369Thr
ENST00000688922.1:c.1026_1027delinsAC
ENST00000693560.1:c.1624_1625delinsAC ENSP00000509861.1:p.Val542Thr
ENST00000371953.8:c.1105_1106delinsAC MANE Select ENSP00000361021.3:p.Val369Thr
ENST00000371953.7:c.1105_1106delinsAC ENSP00000361021.3:p.Val369Thr
NM_000314.5:c.1105_1106delinsAC NP_000305.3:p.Val369Thr
NM_000314.6:c.1105_1106delinsAC NP_000305.3:p.Val369Thr
NM_001304717.2:c.1624_1625delinsAC NP_001291646.2:p.Val542Thr
NM_001304718.1:c.514_515delinsAC NP_001291647.1:p.Val172Thr
XM_006717926.2:c.1060_1061delinsAC XP_006717989.1:p.Val354Thr
XM_011539982.1:c.1009_1010delinsAC XP_011538284.1:p.Val337Thr
XR_945791.1:n.1675_1676delinsAC
NM_000314.7:c.1105_1106delinsAC NP_000305.3:p.Val369Thr
NM_001304717.5:c.1624_1625delinsAC NP_001291646.4:p.Val542Thr
NM_001304718.2:c.514_515delinsAC NP_001291647.1:p.Val172Thr
NM_000314.8:c.1105_1106delinsAC MANE Select NP_000305.3:p.Val369Thr