Canonical Allele Identifier: CA891837981
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965419_87965420delinsTA , CM000672.2:g.87965419_87965420delinsTA GRCh38
NC_000010.10:g.89725176_89725177delinsTA , CM000672.1:g.89725176_89725177delinsTA GRCh37
NC_000010.9:g.89715156_89715157delinsTA NCBI36
NG_007466.2:g.106981_106982delinsTA , LRG_311:g.106981_106982delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1252_1253delinsTA ENSP00000514759.2:p.Pro418Ter
ENST00000710265.1:c.*188_*189delinsTA ENSP00000518161.1:n.*188_*189delinsTA
ENST00000688158.2:n.1894_1895delinsTA
ENST00000688922.2:c.*989_*990delinsTA ENSP00000508742.2:n.*989_*990delinsTA
ENST00000700021.1:c.1114_1115delinsTA ENSP00000514757.1:p.Pro372Ter
ENST00000700022.1:c.*498_*499delinsTA ENSP00000514758.1:n.*498_*499delinsTA
ENST00000700023.1:n.2317_2318delinsTA
ENST00000700024.1:n.2551_2552delinsTA
ENST00000706954.1:c.1159_1160delinsTA ENSP00000516674.1:p.Pro387Ter
ENST00000706955.1:c.*1194_*1195delinsTA ENSP00000516675.1:n.*1194_*1195delinsTA
ENST00000686459.1:c.*745_*746delinsTA ENSP00000508909.1:n.*745_*746delinsTA
ENST00000688158.1:c.*1270_*1271delinsTA ENSP00000509254.1:n.*1270_*1271delinsTA
ENST00000688308.1:c.1159_1160delinsTA ENSP00000508752.1:p.Pro387Ter
ENST00000688922.1:c.1080_1081delinsTA
ENST00000693560.1:c.1678_1679delinsTA ENSP00000509861.1:p.Pro560Ter
ENST00000371953.8:c.1159_1160delinsTA MANE Select ENSP00000361021.3:p.Pro387Ter
ENST00000371953.7:c.1159_1160delinsTA ENSP00000361021.3:p.Pro387Ter
NM_000314.5:c.1159_1160delinsTA NP_000305.3:p.Pro387Ter
NM_000314.6:c.1159_1160delinsTA NP_000305.3:p.Pro387Ter
NM_001304717.2:c.1678_1679delinsTA NP_001291646.2:p.Pro560Ter
NM_001304718.1:c.568_569delinsTA NP_001291647.1:p.Pro190Ter
XM_006717926.2:c.1114_1115delinsTA XP_006717989.1:p.Pro372Ter
XM_011539982.1:c.1063_1064delinsTA XP_011538284.1:p.Pro355Ter
XR_945791.1:n.1729_1730delinsTA
NM_000314.7:c.1159_1160delinsTA NP_000305.3:p.Pro387Ter
NM_001304717.5:c.1678_1679delinsTA NP_001291646.4:p.Pro560Ter
NM_001304718.2:c.568_569delinsTA NP_001291647.1:p.Pro190Ter
NM_000314.8:c.1159_1160delinsTA MANE Select NP_000305.3:p.Pro387Ter