Canonical Allele Identifier: CA891837735
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965386_87965387delinsTG , CM000672.2:g.87965386_87965387delinsTG GRCh38
NC_000010.10:g.89725143_89725144delinsTG , CM000672.1:g.89725143_89725144delinsTG GRCh37
NC_000010.9:g.89715123_89715124delinsTG NCBI36
NG_007466.2:g.106948_106949delinsTG , LRG_311:g.106948_106949delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1219_1220delinsTG ENSP00000514759.2:p.His407Cys
ENST00000710265.1:c.*155_*156delinsTG ENSP00000518161.1:n.*155_*156delinsTG
ENST00000688158.2:n.1861_1862delinsTG
ENST00000688922.2:c.*956_*957delinsTG ENSP00000508742.2:n.*956_*957delinsTG
ENST00000700021.1:c.1081_1082delinsTG ENSP00000514757.1:p.His361Cys
ENST00000700022.1:c.*465_*466delinsTG ENSP00000514758.1:n.*465_*466delinsTG
ENST00000700023.1:n.2284_2285delinsTG
ENST00000700024.1:n.2518_2519delinsTG
ENST00000706954.1:c.1126_1127delinsTG ENSP00000516674.1:p.His376Cys
ENST00000706955.1:c.*1161_*1162delinsTG ENSP00000516675.1:n.*1161_*1162delinsTG
ENST00000686459.1:c.*712_*713delinsTG ENSP00000508909.1:n.*712_*713delinsTG
ENST00000688158.1:c.*1237_*1238delinsTG ENSP00000509254.1:n.*1237_*1238delinsTG
ENST00000688308.1:c.1126_1127delinsTG ENSP00000508752.1:p.His376Cys
ENST00000688922.1:c.1047_1048delinsTG
ENST00000693560.1:c.1645_1646delinsTG ENSP00000509861.1:p.His549Cys
ENST00000371953.8:c.1126_1127delinsTG MANE Select ENSP00000361021.3:p.His376Cys
ENST00000371953.7:c.1126_1127delinsTG ENSP00000361021.3:p.His376Cys
NM_000314.5:c.1126_1127delinsTG NP_000305.3:p.His376Cys
NM_000314.6:c.1126_1127delinsTG NP_000305.3:p.His376Cys
NM_001304717.2:c.1645_1646delinsTG NP_001291646.2:p.His549Cys
NM_001304718.1:c.535_536delinsTG NP_001291647.1:p.His179Cys
XM_006717926.2:c.1081_1082delinsTG XP_006717989.1:p.His361Cys
XM_011539982.1:c.1030_1031delinsTG XP_011538284.1:p.His344Cys
XR_945791.1:n.1696_1697delinsTG
NM_000314.7:c.1126_1127delinsTG NP_000305.3:p.His376Cys
NM_001304717.5:c.1645_1646delinsTG NP_001291646.4:p.His549Cys
NM_001304718.2:c.535_536delinsTG NP_001291647.1:p.His179Cys
NM_000314.8:c.1126_1127delinsTG MANE Select NP_000305.3:p.His376Cys