Canonical Allele Identifier: CA891840895
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957990_87957991delinsCG , CM000672.2:g.87957990_87957991delinsCG GRCh38
NC_000010.10:g.89717747_89717748delinsCG , CM000672.1:g.89717747_89717748delinsCG GRCh37
NC_000010.9:g.89707727_89707728delinsCG NCBI36
NG_007466.2:g.99552_99553delinsCG , LRG_311:g.99552_99553delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.772_773delinsCG ENSP00000514759.2:p.Phe258Arg
ENST00000710265.1:c.772_773delinsCG ENSP00000518161.1:p.Phe258Arg
ENST00000472832.3:c.772_773delinsCG ENSP00000483066.2:p.Phe258Arg
ENST00000688158.2:n.1507_1508delinsCG
ENST00000688922.2:c.*602_*603delinsCG ENSP00000508742.2:n.*602_*603delinsCG
ENST00000700021.1:c.727_728delinsCG ENSP00000514757.1:p.Phe243Arg
ENST00000700022.1:c.*111_*112delinsCG ENSP00000514758.1:n.*111_*112delinsCG
ENST00000700023.1:n.1930_1931delinsCG
ENST00000700024.1:n.2164_2165delinsCG
ENST00000700025.1:n.1541_1542delinsCG
ENST00000700026.1:n.409_410delinsCG
ENST00000700029.1:c.606_607delinsCG
ENST00000706954.1:c.772_773delinsCG ENSP00000516674.1:p.Phe258Arg
ENST00000706955.1:c.*807_*808delinsCG ENSP00000516675.1:n.*807_*808delinsCG
ENST00000686459.1:c.*358_*359delinsCG ENSP00000508909.1:n.*358_*359delinsCG
ENST00000688158.1:c.*883_*884delinsCG ENSP00000509254.1:n.*883_*884delinsCG
ENST00000688308.1:c.772_773delinsCG ENSP00000508752.1:p.Phe258Arg
ENST00000688922.1:c.693_694delinsCG
ENST00000693560.1:c.1291_1292delinsCG ENSP00000509861.1:p.Phe431Arg
ENST00000371953.8:c.772_773delinsCG MANE Select ENSP00000361021.3:p.Phe258Arg
ENST00000371953.7:c.772_773delinsCG ENSP00000361021.3:p.Phe258Arg
ENST00000472832.2:c.199_200delinsCG ENSP00000483066.1:p.Phe67Arg
NM_000314.5:c.772_773delinsCG NP_000305.3:p.Phe258Arg
NM_000314.6:c.772_773delinsCG NP_000305.3:p.Phe258Arg
NM_001304717.2:c.1291_1292delinsCG NP_001291646.2:p.Phe431Arg
NM_001304718.1:c.181_182delinsCG NP_001291647.1:p.Phe61Arg
XM_006717926.2:c.727_728delinsCG XP_006717989.1:p.Phe243Arg
XM_011539981.1:c.772_773delinsCG XP_011538283.1:p.Phe258Arg
XM_011539982.1:c.676_677delinsCG XP_011538284.1:p.Phe226Arg
XR_945791.1:n.1342_1343delinsCG
NM_000314.7:c.772_773delinsCG NP_000305.3:p.Phe258Arg
NM_001304717.5:c.1291_1292delinsCG NP_001291646.4:p.Phe431Arg
NM_001304718.2:c.181_182delinsCG NP_001291647.1:p.Phe61Arg
NM_000314.8:c.772_773delinsCG MANE Select NP_000305.3:p.Phe258Arg