Canonical Allele Identifier: CA891838040
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965425_87965427delinsTTG , CM000672.2:g.87965425_87965427delinsTTG GRCh38
NC_000010.10:g.89725182_89725184delinsTTG , CM000672.1:g.89725182_89725184delinsTTG GRCh37
NC_000010.9:g.89715162_89715164delinsTTG NCBI36
NG_007466.2:g.106987_106989delinsTTG , LRG_311:g.106987_106989delinsTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1258_1260delinsTTG ENSP00000514759.2:p.Asn420Leu
ENST00000710265.1:c.*194_*196delinsTTG ENSP00000518161.1:n.*194_*196delinsTTG
ENST00000688158.2:n.1900_1902delinsTTG
ENST00000688922.2:c.*995_*997delinsTTG ENSP00000508742.2:n.*995_*997delinsTTG
ENST00000700021.1:c.1120_1122delinsTTG ENSP00000514757.1:p.Asn374Leu
ENST00000700022.1:c.*504_*506delinsTTG ENSP00000514758.1:n.*504_*506delinsTTG
ENST00000700023.1:n.2323_2325delinsTTG
ENST00000700024.1:n.2557_2559delinsTTG
ENST00000706954.1:c.1165_1167delinsTTG ENSP00000516674.1:p.Asn389Leu
ENST00000706955.1:c.*1200_*1202delinsTTG ENSP00000516675.1:n.*1200_*1202delinsTTG
ENST00000686459.1:c.*751_*753delinsTTG ENSP00000508909.1:n.*751_*753delinsTTG
ENST00000688158.1:c.*1276_*1278delinsTTG ENSP00000509254.1:n.*1276_*1278delinsTTG
ENST00000688308.1:c.1165_1167delinsTTG ENSP00000508752.1:p.Asn389Leu
ENST00000688922.1:c.1086_1088delinsTTG
ENST00000693560.1:c.1684_1686delinsTTG ENSP00000509861.1:p.Asn562Leu
ENST00000371953.8:c.1165_1167delinsTTG MANE Select ENSP00000361021.3:p.Asn389Leu
ENST00000371953.7:c.1165_1167delinsTTG ENSP00000361021.3:p.Asn389Leu
NM_000314.5:c.1165_1167delinsTTG NP_000305.3:p.Asn389Leu
NM_000314.6:c.1165_1167delinsTTG NP_000305.3:p.Asn389Leu
NM_001304717.2:c.1684_1686delinsTTG NP_001291646.2:p.Asn562Leu
NM_001304718.1:c.574_576delinsTTG NP_001291647.1:p.Asn192Leu
XM_006717926.2:c.1120_1122delinsTTG XP_006717989.1:p.Asn374Leu
XM_011539982.1:c.1069_1071delinsTTG XP_011538284.1:p.Asn357Leu
XR_945791.1:n.1735_1737delinsTTG
NM_000314.7:c.1165_1167delinsTTG NP_000305.3:p.Asn389Leu
NM_001304717.5:c.1684_1686delinsTTG NP_001291646.4:p.Asn562Leu
NM_001304718.2:c.574_576delinsTTG NP_001291647.1:p.Asn192Leu
NM_000314.8:c.1165_1167delinsTTG MANE Select NP_000305.3:p.Asn389Leu