Canonical Allele Identifier: CA891835890
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87864510_87864511delinsCT , CM000672.2:g.87864510_87864511delinsCT GRCh38
NC_000010.10:g.89624267_89624268delinsCT , CM000672.1:g.89624267_89624268delinsCT GRCh37
NC_000010.9:g.89614247_89614248delinsCT NCBI36
NG_007466.2:g.6072_6073delinsCT , LRG_311:g.6072_6073delinsCT
NG_033079.1:g.3927_3928delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.41_42delinsCT ENSP00000514759.2:p.Arg14Thr
ENST00000710265.1:c.41_42delinsCT ENSP00000518161.1:p.Arg14Thr
ENST00000472832.3:c.41_42delinsCT ENSP00000483066.2:p.Arg14Thr
ENST00000688922.2:c.41_42delinsCT ENSP00000508742.2:p.Arg14Thr
ENST00000700021.1:c.41_42delinsCT ENSP00000514757.1:p.Arg14Thr
ENST00000700022.1:c.41_42delinsCT ENSP00000514758.1:p.Arg14Thr
ENST00000706954.1:c.41_42delinsCT ENSP00000516674.1:p.Arg14Thr
ENST00000706955.1:c.41_42delinsCT ENSP00000516675.1:p.Arg14Thr
ENST00000686459.1:c.41_42delinsCT ENSP00000508909.1:p.Arg14Thr
ENST00000688158.1:c.41_42delinsCT ENSP00000509254.1:p.Arg14Thr
ENST00000688308.1:c.41_42delinsCT ENSP00000508752.1:p.Arg14Thr
ENST00000693560.1:c.560_561delinsCT ENSP00000509861.1:p.Arg187Thr
ENST00000371953.8:c.41_42delinsCT MANE Select ENSP00000361021.3:p.Arg14Thr
ENST00000371953.7:c.41_42delinsCT ENSP00000361021.3:p.Arg14Thr
ENST00000462694.1:n.43_44delinsCT
ENST00000487939.1:n.62_63delinsCT
ENST00000610634.1:c.-62_-61delinsCT ENSP00000477517.1:n.-62_-61delinsCT
ENST00000618586.1:n.10_11delinsCT
NM_000314.5:c.41_42delinsCT NP_000305.3:p.Arg14Thr
NM_000314.6:c.41_42delinsCT NP_000305.3:p.Arg14Thr
NM_001304717.2:c.560_561delinsCT NP_001291646.2:p.Arg187Thr
NM_001304718.1:c.-665_-664delinsCT NP_001291647.1:n.-665_-664delinsCT
XM_006717926.2:c.41_42delinsCT XP_006717989.1:p.Arg14Thr
XM_011539981.1:c.41_42delinsCT XP_011538283.1:p.Arg14Thr
XR_945789.1:n.753_754delinsCT
XR_945790.1:n.753_754delinsCT
XR_945791.1:n.753_754delinsCT
NM_000314.7:c.41_42delinsCT NP_000305.3:p.Arg14Thr
NM_001304717.5:c.560_561delinsCT NP_001291646.4:p.Arg187Thr
NM_001304718.2:c.-665_-664delinsCT NP_001291647.1:n.-665_-664delinsCT
NM_000314.8:c.41_42delinsCT MANE Select NP_000305.3:p.Arg14Thr