Canonical Allele Identifier: CA891841636
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965410_87965411delinsCT , CM000672.2:g.87965410_87965411delinsCT GRCh38
NC_000010.10:g.89725167_89725168delinsCT , CM000672.1:g.89725167_89725168delinsCT GRCh37
NC_000010.9:g.89715147_89715148delinsCT NCBI36
NG_007466.2:g.106972_106973delinsCT , LRG_311:g.106972_106973delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1243_1244delinsCT ENSP00000514759.2:p.Asp415Leu
ENST00000710265.1:c.*179_*180delinsCT ENSP00000518161.1:n.*179_*180delinsCT
ENST00000688158.2:n.1885_1886delinsCT
ENST00000688922.2:c.*980_*981delinsCT ENSP00000508742.2:n.*980_*981delinsCT
ENST00000700021.1:c.1105_1106delinsCT ENSP00000514757.1:p.Asp369Leu
ENST00000700022.1:c.*489_*490delinsCT ENSP00000514758.1:n.*489_*490delinsCT
ENST00000700023.1:n.2308_2309delinsCT
ENST00000700024.1:n.2542_2543delinsCT
ENST00000706954.1:c.1150_1151delinsCT ENSP00000516674.1:p.Asp384Leu
ENST00000706955.1:c.*1185_*1186delinsCT ENSP00000516675.1:n.*1185_*1186delinsCT
ENST00000686459.1:c.*736_*737delinsCT ENSP00000508909.1:n.*736_*737delinsCT
ENST00000688158.1:c.*1261_*1262delinsCT ENSP00000509254.1:n.*1261_*1262delinsCT
ENST00000688308.1:c.1150_1151delinsCT ENSP00000508752.1:p.Asp384Leu
ENST00000688922.1:c.1071_1072delinsCT
ENST00000693560.1:c.1669_1670delinsCT ENSP00000509861.1:p.Asp557Leu
ENST00000371953.8:c.1150_1151delinsCT MANE Select ENSP00000361021.3:p.Asp384Leu
ENST00000371953.7:c.1150_1151delinsCT ENSP00000361021.3:p.Asp384Leu
NM_000314.5:c.1150_1151delinsCT NP_000305.3:p.Asp384Leu
NM_000314.6:c.1150_1151delinsCT NP_000305.3:p.Asp384Leu
NM_001304717.2:c.1669_1670delinsCT NP_001291646.2:p.Asp557Leu
NM_001304718.1:c.559_560delinsCT NP_001291647.1:p.Asp187Leu
XM_006717926.2:c.1105_1106delinsCT XP_006717989.1:p.Asp369Leu
XM_011539982.1:c.1054_1055delinsCT XP_011538284.1:p.Asp352Leu
XR_945791.1:n.1720_1721delinsCT
NM_000314.7:c.1150_1151delinsCT NP_000305.3:p.Asp384Leu
NM_001304717.5:c.1669_1670delinsCT NP_001291646.4:p.Asp557Leu
NM_001304718.2:c.559_560delinsCT NP_001291647.1:p.Asp187Leu
NM_000314.8:c.1150_1151delinsCT MANE Select NP_000305.3:p.Asp384Leu