Canonical Allele Identifier: CA891835865
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87864509_87864511delinsGGT , CM000672.2:g.87864509_87864511delinsGGT GRCh38
NC_000010.10:g.89624266_89624268delinsGGT , CM000672.1:g.89624266_89624268delinsGGT GRCh37
NC_000010.9:g.89614246_89614248delinsGGT NCBI36
NG_007466.2:g.6071_6073delinsGGT , LRG_311:g.6071_6073delinsGGT
NG_033079.1:g.3927_3929delinsACC

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.40_42delinsGGT ENSP00000514759.2:p.Arg14Gly
ENST00000710265.1:c.40_42delinsGGT ENSP00000518161.1:p.Arg14Gly
ENST00000472832.3:c.40_42delinsGGT ENSP00000483066.2:p.Arg14Gly
ENST00000688922.2:c.40_42delinsGGT ENSP00000508742.2:p.Arg14Gly
ENST00000700021.1:c.40_42delinsGGT ENSP00000514757.1:p.Arg14Gly
ENST00000700022.1:c.40_42delinsGGT ENSP00000514758.1:p.Arg14Gly
ENST00000706954.1:c.40_42delinsGGT ENSP00000516674.1:p.Arg14Gly
ENST00000706955.1:c.40_42delinsGGT ENSP00000516675.1:p.Arg14Gly
ENST00000686459.1:c.40_42delinsGGT ENSP00000508909.1:p.Arg14Gly
ENST00000688158.1:c.40_42delinsGGT ENSP00000509254.1:p.Arg14Gly
ENST00000688308.1:c.40_42delinsGGT ENSP00000508752.1:p.Arg14Gly
ENST00000693560.1:c.559_561delinsGGT ENSP00000509861.1:p.Arg187Gly
ENST00000371953.8:c.40_42delinsGGT MANE Select ENSP00000361021.3:p.Arg14Gly
ENST00000371953.7:c.40_42delinsGGT ENSP00000361021.3:p.Arg14Gly
ENST00000462694.1:n.42_44delinsGGT
ENST00000487939.1:n.61_63delinsGGT
ENST00000610634.1:c.-63_-61delinsGGT ENSP00000477517.1:n.-63_-61delinsGGT
ENST00000618586.1:n.9_11delinsGGT
NM_000314.5:c.40_42delinsGGT NP_000305.3:p.Arg14Gly
NM_000314.6:c.40_42delinsGGT NP_000305.3:p.Arg14Gly
NM_001304717.2:c.559_561delinsGGT NP_001291646.2:p.Arg187Gly
NM_001304718.1:c.-666_-664delinsGGT NP_001291647.1:n.-666_-664delinsGGT
XM_006717926.2:c.40_42delinsGGT XP_006717989.1:p.Arg14Gly
XM_011539981.1:c.40_42delinsGGT XP_011538283.1:p.Arg14Gly
XR_945789.1:n.752_754delinsGGT
XR_945790.1:n.752_754delinsGGT
XR_945791.1:n.752_754delinsGGT
NM_000314.7:c.40_42delinsGGT NP_000305.3:p.Arg14Gly
NM_001304717.5:c.559_561delinsGGT NP_001291646.4:p.Arg187Gly
NM_001304718.2:c.-666_-664delinsGGT NP_001291647.1:n.-666_-664delinsGGT
NM_000314.8:c.40_42delinsGGT MANE Select NP_000305.3:p.Arg14Gly