Canonical Allele Identifier: CA891840896
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957990_87957991delinsCC , CM000672.2:g.87957990_87957991delinsCC GRCh38
NC_000010.10:g.89717747_89717748delinsCC , CM000672.1:g.89717747_89717748delinsCC GRCh37
NC_000010.9:g.89707727_89707728delinsCC NCBI36
NG_007466.2:g.99552_99553delinsCC , LRG_311:g.99552_99553delinsCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.772_773delinsCC ENSP00000514759.2:p.Phe258Pro
ENST00000710265.1:c.772_773delinsCC ENSP00000518161.1:p.Phe258Pro
ENST00000472832.3:c.772_773delinsCC ENSP00000483066.2:p.Phe258Pro
ENST00000688158.2:n.1507_1508delinsCC
ENST00000688922.2:c.*602_*603delinsCC ENSP00000508742.2:n.*602_*603delinsCC
ENST00000700021.1:c.727_728delinsCC ENSP00000514757.1:p.Phe243Pro
ENST00000700022.1:c.*111_*112delinsCC ENSP00000514758.1:n.*111_*112delinsCC
ENST00000700023.1:n.1930_1931delinsCC
ENST00000700024.1:n.2164_2165delinsCC
ENST00000700025.1:n.1541_1542delinsCC
ENST00000700026.1:n.409_410delinsCC
ENST00000700029.1:c.606_607delinsCC
ENST00000706954.1:c.772_773delinsCC ENSP00000516674.1:p.Phe258Pro
ENST00000706955.1:c.*807_*808delinsCC ENSP00000516675.1:n.*807_*808delinsCC
ENST00000686459.1:c.*358_*359delinsCC ENSP00000508909.1:n.*358_*359delinsCC
ENST00000688158.1:c.*883_*884delinsCC ENSP00000509254.1:n.*883_*884delinsCC
ENST00000688308.1:c.772_773delinsCC ENSP00000508752.1:p.Phe258Pro
ENST00000688922.1:c.693_694delinsCC
ENST00000693560.1:c.1291_1292delinsCC ENSP00000509861.1:p.Phe431Pro
ENST00000371953.8:c.772_773delinsCC MANE Select ENSP00000361021.3:p.Phe258Pro
ENST00000371953.7:c.772_773delinsCC ENSP00000361021.3:p.Phe258Pro
ENST00000472832.2:c.199_200delinsCC ENSP00000483066.1:p.Phe67Pro
NM_000314.5:c.772_773delinsCC NP_000305.3:p.Phe258Pro
NM_000314.6:c.772_773delinsCC NP_000305.3:p.Phe258Pro
NM_001304717.2:c.1291_1292delinsCC NP_001291646.2:p.Phe431Pro
NM_001304718.1:c.181_182delinsCC NP_001291647.1:p.Phe61Pro
XM_006717926.2:c.727_728delinsCC XP_006717989.1:p.Phe243Pro
XM_011539981.1:c.772_773delinsCC XP_011538283.1:p.Phe258Pro
XM_011539982.1:c.676_677delinsCC XP_011538284.1:p.Phe226Pro
XR_945791.1:n.1342_1343delinsCC
NM_000314.7:c.772_773delinsCC NP_000305.3:p.Phe258Pro
NM_001304717.5:c.1291_1292delinsCC NP_001291646.4:p.Phe431Pro
NM_001304718.2:c.181_182delinsCC NP_001291647.1:p.Phe61Pro
NM_000314.8:c.772_773delinsCC MANE Select NP_000305.3:p.Phe258Pro