Canonical Allele Identifier: CA891841645
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965416_87965417delinsCC , CM000672.2:g.87965416_87965417delinsCC GRCh38
NC_000010.10:g.89725173_89725174delinsCC , CM000672.1:g.89725173_89725174delinsCC GRCh37
NC_000010.9:g.89715153_89715154delinsCC NCBI36
NG_007466.2:g.106978_106979delinsCC , LRG_311:g.106978_106979delinsCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1249_1250delinsCC ENSP00000514759.2:p.Asp417Pro
ENST00000710265.1:c.*185_*186delinsCC ENSP00000518161.1:n.*185_*186delinsCC
ENST00000688158.2:n.1891_1892delinsCC
ENST00000688922.2:c.*986_*987delinsCC ENSP00000508742.2:n.*986_*987delinsCC
ENST00000700021.1:c.1111_1112delinsCC ENSP00000514757.1:p.Asp371Pro
ENST00000700022.1:c.*495_*496delinsCC ENSP00000514758.1:n.*495_*496delinsCC
ENST00000700023.1:n.2314_2315delinsCC
ENST00000700024.1:n.2548_2549delinsCC
ENST00000706954.1:c.1156_1157delinsCC ENSP00000516674.1:p.Asp386Pro
ENST00000706955.1:c.*1191_*1192delinsCC ENSP00000516675.1:n.*1191_*1192delinsCC
ENST00000686459.1:c.*742_*743delinsCC ENSP00000508909.1:n.*742_*743delinsCC
ENST00000688158.1:c.*1267_*1268delinsCC ENSP00000509254.1:n.*1267_*1268delinsCC
ENST00000688308.1:c.1156_1157delinsCC ENSP00000508752.1:p.Asp386Pro
ENST00000688922.1:c.1077_1078delinsCC
ENST00000693560.1:c.1675_1676delinsCC ENSP00000509861.1:p.Asp559Pro
ENST00000371953.8:c.1156_1157delinsCC MANE Select ENSP00000361021.3:p.Asp386Pro
ENST00000371953.7:c.1156_1157delinsCC ENSP00000361021.3:p.Asp386Pro
NM_000314.5:c.1156_1157delinsCC NP_000305.3:p.Asp386Pro
NM_000314.6:c.1156_1157delinsCC NP_000305.3:p.Asp386Pro
NM_001304717.2:c.1675_1676delinsCC NP_001291646.2:p.Asp559Pro
NM_001304718.1:c.565_566delinsCC NP_001291647.1:p.Asp189Pro
XM_006717926.2:c.1111_1112delinsCC XP_006717989.1:p.Asp371Pro
XM_011539982.1:c.1060_1061delinsCC XP_011538284.1:p.Asp354Pro
XR_945791.1:n.1726_1727delinsCC
NM_000314.7:c.1156_1157delinsCC NP_000305.3:p.Asp386Pro
NM_001304717.5:c.1675_1676delinsCC NP_001291646.4:p.Asp559Pro
NM_001304718.2:c.565_566delinsCC NP_001291647.1:p.Asp189Pro
NM_000314.8:c.1156_1157delinsCC MANE Select NP_000305.3:p.Asp386Pro