Canonical Allele Identifier: CA891837657
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965377_87965378delinsCC , CM000672.2:g.87965377_87965378delinsCC GRCh38
NC_000010.10:g.89725134_89725135delinsCC , CM000672.1:g.89725134_89725135delinsCC GRCh37
NC_000010.9:g.89715114_89715115delinsCC NCBI36
NG_007466.2:g.106939_106940delinsCC , LRG_311:g.106939_106940delinsCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1210_1211delinsCC ENSP00000514759.2:p.Glu404Pro
ENST00000710265.1:c.*146_*147delinsCC ENSP00000518161.1:n.*146_*147delinsCC
ENST00000688158.2:n.1852_1853delinsCC
ENST00000688922.2:c.*947_*948delinsCC ENSP00000508742.2:n.*947_*948delinsCC
ENST00000700021.1:c.1072_1073delinsCC ENSP00000514757.1:p.Glu358Pro
ENST00000700022.1:c.*456_*457delinsCC ENSP00000514758.1:n.*456_*457delinsCC
ENST00000700023.1:n.2275_2276delinsCC
ENST00000700024.1:n.2509_2510delinsCC
ENST00000706954.1:c.1117_1118delinsCC ENSP00000516674.1:p.Glu373Pro
ENST00000706955.1:c.*1152_*1153delinsCC ENSP00000516675.1:n.*1152_*1153delinsCC
ENST00000686459.1:c.*703_*704delinsCC ENSP00000508909.1:n.*703_*704delinsCC
ENST00000688158.1:c.*1228_*1229delinsCC ENSP00000509254.1:n.*1228_*1229delinsCC
ENST00000688308.1:c.1117_1118delinsCC ENSP00000508752.1:p.Glu373Pro
ENST00000688922.1:c.1038_1039delinsCC
ENST00000693560.1:c.1636_1637delinsCC ENSP00000509861.1:p.Glu546Pro
ENST00000371953.8:c.1117_1118delinsCC MANE Select ENSP00000361021.3:p.Glu373Pro
ENST00000371953.7:c.1117_1118delinsCC ENSP00000361021.3:p.Glu373Pro
NM_000314.5:c.1117_1118delinsCC NP_000305.3:p.Glu373Pro
NM_000314.6:c.1117_1118delinsCC NP_000305.3:p.Glu373Pro
NM_001304717.2:c.1636_1637delinsCC NP_001291646.2:p.Glu546Pro
NM_001304718.1:c.526_527delinsCC NP_001291647.1:p.Glu176Pro
XM_006717926.2:c.1072_1073delinsCC XP_006717989.1:p.Glu358Pro
XM_011539982.1:c.1021_1022delinsCC XP_011538284.1:p.Glu341Pro
XR_945791.1:n.1687_1688delinsCC
NM_000314.7:c.1117_1118delinsCC NP_000305.3:p.Glu373Pro
NM_001304717.5:c.1636_1637delinsCC NP_001291646.4:p.Glu546Pro
NM_001304718.2:c.526_527delinsCC NP_001291647.1:p.Glu176Pro
NM_000314.8:c.1117_1118delinsCC MANE Select NP_000305.3:p.Glu373Pro