Canonical Allele Identifier: CA891840839
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957975_87957976delinsCG , CM000672.2:g.87957975_87957976delinsCG GRCh38
NC_000010.10:g.89717732_89717733delinsCG , CM000672.1:g.89717732_89717733delinsCG GRCh37
NC_000010.9:g.89707712_89707713delinsCG NCBI36
NG_007466.2:g.99537_99538delinsCG , LRG_311:g.99537_99538delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.757_758delinsCG ENSP00000514759.2:p.Ile253Arg
ENST00000710265.1:c.757_758delinsCG ENSP00000518161.1:p.Ile253Arg
ENST00000472832.3:c.757_758delinsCG ENSP00000483066.2:p.Ile253Arg
ENST00000688158.2:n.1492_1493delinsCG
ENST00000688922.2:c.*587_*588delinsCG ENSP00000508742.2:n.*587_*588delinsCG
ENST00000700021.1:c.712_713delinsCG ENSP00000514757.1:p.Ile238Arg
ENST00000700022.1:c.*96_*97delinsCG ENSP00000514758.1:n.*96_*97delinsCG
ENST00000700023.1:n.1915_1916delinsCG
ENST00000700024.1:n.2149_2150delinsCG
ENST00000700025.1:n.1526_1527delinsCG
ENST00000700026.1:n.394_395delinsCG
ENST00000700029.1:c.591_592delinsCG
ENST00000706954.1:c.757_758delinsCG ENSP00000516674.1:p.Ile253Arg
ENST00000706955.1:c.*792_*793delinsCG ENSP00000516675.1:n.*792_*793delinsCG
ENST00000686459.1:c.*343_*344delinsCG ENSP00000508909.1:n.*343_*344delinsCG
ENST00000688158.1:c.*868_*869delinsCG ENSP00000509254.1:n.*868_*869delinsCG
ENST00000688308.1:c.757_758delinsCG ENSP00000508752.1:p.Ile253Arg
ENST00000688922.1:c.678_679delinsCG
ENST00000693560.1:c.1276_1277delinsCG ENSP00000509861.1:p.Ile426Arg
ENST00000371953.8:c.757_758delinsCG MANE Select ENSP00000361021.3:p.Ile253Arg
ENST00000371953.7:c.757_758delinsCG ENSP00000361021.3:p.Ile253Arg
ENST00000472832.2:c.184_185delinsCG ENSP00000483066.1:p.Ile62Arg
NM_000314.5:c.757_758delinsCG NP_000305.3:p.Ile253Arg
NM_000314.6:c.757_758delinsCG NP_000305.3:p.Ile253Arg
NM_001304717.2:c.1276_1277delinsCG NP_001291646.2:p.Ile426Arg
NM_001304718.1:c.166_167delinsCG NP_001291647.1:p.Ile56Arg
XM_006717926.2:c.712_713delinsCG XP_006717989.1:p.Ile238Arg
XM_011539981.1:c.757_758delinsCG XP_011538283.1:p.Ile253Arg
XM_011539982.1:c.661_662delinsCG XP_011538284.1:p.Ile221Arg
XR_945791.1:n.1327_1328delinsCG
NM_000314.7:c.757_758delinsCG NP_000305.3:p.Ile253Arg
NM_001304717.5:c.1276_1277delinsCG NP_001291646.4:p.Ile426Arg
NM_001304718.2:c.166_167delinsCG NP_001291647.1:p.Ile56Arg
NM_000314.8:c.757_758delinsCG MANE Select NP_000305.3:p.Ile253Arg