Canonical Allele Identifier: CA891837940
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965410_87965412delinsACT , CM000672.2:g.87965410_87965412delinsACT GRCh38
NC_000010.10:g.89725167_89725169delinsACT , CM000672.1:g.89725167_89725169delinsACT GRCh37
NC_000010.9:g.89715147_89715149delinsACT NCBI36
NG_007466.2:g.106972_106974delinsACT , LRG_311:g.106972_106974delinsACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1243_1245delinsACT ENSP00000514759.2:p.Asp415Thr
ENST00000710265.1:c.*179_*181delinsACT ENSP00000518161.1:n.*179_*181delinsACT
ENST00000688158.2:n.1885_1887delinsACT
ENST00000688922.2:c.*980_*982delinsACT ENSP00000508742.2:n.*980_*982delinsACT
ENST00000700021.1:c.1105_1107delinsACT ENSP00000514757.1:p.Asp369Thr
ENST00000700022.1:c.*489_*491delinsACT ENSP00000514758.1:n.*489_*491delinsACT
ENST00000700023.1:n.2308_2310delinsACT
ENST00000700024.1:n.2542_2544delinsACT
ENST00000706954.1:c.1150_1152delinsACT ENSP00000516674.1:p.Asp384Thr
ENST00000706955.1:c.*1185_*1187delinsACT ENSP00000516675.1:n.*1185_*1187delinsACT
ENST00000686459.1:c.*736_*738delinsACT ENSP00000508909.1:n.*736_*738delinsACT
ENST00000688158.1:c.*1261_*1263delinsACT ENSP00000509254.1:n.*1261_*1263delinsACT
ENST00000688308.1:c.1150_1152delinsACT ENSP00000508752.1:p.Asp384Thr
ENST00000688922.1:c.1071_1073delinsACT
ENST00000693560.1:c.1669_1671delinsACT ENSP00000509861.1:p.Asp557Thr
ENST00000371953.8:c.1150_1152delinsACT MANE Select ENSP00000361021.3:p.Asp384Thr
ENST00000371953.7:c.1150_1152delinsACT ENSP00000361021.3:p.Asp384Thr
NM_000314.5:c.1150_1152delinsACT NP_000305.3:p.Asp384Thr
NM_000314.6:c.1150_1152delinsACT NP_000305.3:p.Asp384Thr
NM_001304717.2:c.1669_1671delinsACT NP_001291646.2:p.Asp557Thr
NM_001304718.1:c.559_561delinsACT NP_001291647.1:p.Asp187Thr
XM_006717926.2:c.1105_1107delinsACT XP_006717989.1:p.Asp369Thr
XM_011539982.1:c.1054_1056delinsACT XP_011538284.1:p.Asp352Thr
XR_945791.1:n.1720_1722delinsACT
NM_000314.7:c.1150_1152delinsACT NP_000305.3:p.Asp384Thr
NM_001304717.5:c.1669_1671delinsACT NP_001291646.4:p.Asp557Thr
NM_001304718.2:c.559_561delinsACT NP_001291647.1:p.Asp187Thr
NM_000314.8:c.1150_1152delinsACT MANE Select NP_000305.3:p.Asp384Thr