Canonical Allele Identifier: CA891837984
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965419_87965420delinsAA , CM000672.2:g.87965419_87965420delinsAA GRCh38
NC_000010.10:g.89725176_89725177delinsAA , CM000672.1:g.89725176_89725177delinsAA GRCh37
NC_000010.9:g.89715156_89715157delinsAA NCBI36
NG_007466.2:g.106981_106982delinsAA , LRG_311:g.106981_106982delinsAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1252_1253delinsAA ENSP00000514759.2:p.Pro418Lys
ENST00000710265.1:c.*188_*189delinsAA ENSP00000518161.1:n.*188_*189delinsAA
ENST00000688158.2:n.1894_1895delinsAA
ENST00000688922.2:c.*989_*990delinsAA ENSP00000508742.2:n.*989_*990delinsAA
ENST00000700021.1:c.1114_1115delinsAA ENSP00000514757.1:p.Pro372Lys
ENST00000700022.1:c.*498_*499delinsAA ENSP00000514758.1:n.*498_*499delinsAA
ENST00000700023.1:n.2317_2318delinsAA
ENST00000700024.1:n.2551_2552delinsAA
ENST00000706954.1:c.1159_1160delinsAA ENSP00000516674.1:p.Pro387Lys
ENST00000706955.1:c.*1194_*1195delinsAA ENSP00000516675.1:n.*1194_*1195delinsAA
ENST00000686459.1:c.*745_*746delinsAA ENSP00000508909.1:n.*745_*746delinsAA
ENST00000688158.1:c.*1270_*1271delinsAA ENSP00000509254.1:n.*1270_*1271delinsAA
ENST00000688308.1:c.1159_1160delinsAA ENSP00000508752.1:p.Pro387Lys
ENST00000688922.1:c.1080_1081delinsAA
ENST00000693560.1:c.1678_1679delinsAA ENSP00000509861.1:p.Pro560Lys
ENST00000371953.8:c.1159_1160delinsAA MANE Select ENSP00000361021.3:p.Pro387Lys
ENST00000371953.7:c.1159_1160delinsAA ENSP00000361021.3:p.Pro387Lys
NM_000314.5:c.1159_1160delinsAA NP_000305.3:p.Pro387Lys
NM_000314.6:c.1159_1160delinsAA NP_000305.3:p.Pro387Lys
NM_001304717.2:c.1678_1679delinsAA NP_001291646.2:p.Pro560Lys
NM_001304718.1:c.568_569delinsAA NP_001291647.1:p.Pro190Lys
XM_006717926.2:c.1114_1115delinsAA XP_006717989.1:p.Pro372Lys
XM_011539982.1:c.1063_1064delinsAA XP_011538284.1:p.Pro355Lys
XR_945791.1:n.1729_1730delinsAA
NM_000314.7:c.1159_1160delinsAA NP_000305.3:p.Pro387Lys
NM_001304717.5:c.1678_1679delinsAA NP_001291646.4:p.Pro560Lys
NM_001304718.2:c.568_569delinsAA NP_001291647.1:p.Pro190Lys
NM_000314.8:c.1159_1160delinsAA MANE Select NP_000305.3:p.Pro387Lys