Canonical Allele Identifier: CA891841613
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965371_87965372delinsCG , CM000672.2:g.87965371_87965372delinsCG GRCh38
NC_000010.10:g.89725128_89725129delinsCG , CM000672.1:g.89725128_89725129delinsCG GRCh37
NC_000010.9:g.89715108_89715109delinsCG NCBI36
NG_007466.2:g.106933_106934delinsCG , LRG_311:g.106933_106934delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1204_1205delinsCG ENSP00000514759.2:p.Asp402Arg
ENST00000710265.1:c.*140_*141delinsCG ENSP00000518161.1:n.*140_*141delinsCG
ENST00000688158.2:n.1846_1847delinsCG
ENST00000688922.2:c.*941_*942delinsCG ENSP00000508742.2:n.*941_*942delinsCG
ENST00000700021.1:c.1066_1067delinsCG ENSP00000514757.1:p.Asp356Arg
ENST00000700022.1:c.*450_*451delinsCG ENSP00000514758.1:n.*450_*451delinsCG
ENST00000700023.1:n.2269_2270delinsCG
ENST00000700024.1:n.2503_2504delinsCG
ENST00000706954.1:c.1111_1112delinsCG ENSP00000516674.1:p.Asp371Arg
ENST00000706955.1:c.*1146_*1147delinsCG ENSP00000516675.1:n.*1146_*1147delinsCG
ENST00000686459.1:c.*697_*698delinsCG ENSP00000508909.1:n.*697_*698delinsCG
ENST00000688158.1:c.*1222_*1223delinsCG ENSP00000509254.1:n.*1222_*1223delinsCG
ENST00000688308.1:c.1111_1112delinsCG ENSP00000508752.1:p.Asp371Arg
ENST00000688922.1:c.1032_1033delinsCG
ENST00000693560.1:c.1630_1631delinsCG ENSP00000509861.1:p.Asp544Arg
ENST00000371953.8:c.1111_1112delinsCG MANE Select ENSP00000361021.3:p.Asp371Arg
ENST00000371953.7:c.1111_1112delinsCG ENSP00000361021.3:p.Asp371Arg
NM_000314.5:c.1111_1112delinsCG NP_000305.3:p.Asp371Arg
NM_000314.6:c.1111_1112delinsCG NP_000305.3:p.Asp371Arg
NM_001304717.2:c.1630_1631delinsCG NP_001291646.2:p.Asp544Arg
NM_001304718.1:c.520_521delinsCG NP_001291647.1:p.Asp174Arg
XM_006717926.2:c.1066_1067delinsCG XP_006717989.1:p.Asp356Arg
XM_011539982.1:c.1015_1016delinsCG XP_011538284.1:p.Asp339Arg
XR_945791.1:n.1681_1682delinsCG
NM_000314.7:c.1111_1112delinsCG NP_000305.3:p.Asp371Arg
NM_001304717.5:c.1630_1631delinsCG NP_001291646.4:p.Asp544Arg
NM_001304718.2:c.520_521delinsCG NP_001291647.1:p.Asp174Arg
NM_000314.8:c.1111_1112delinsCG MANE Select NP_000305.3:p.Asp371Arg