Canonical Allele Identifier: CA891837985
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965419_87965420delinsAG , CM000672.2:g.87965419_87965420delinsAG GRCh38
NC_000010.10:g.89725176_89725177delinsAG , CM000672.1:g.89725176_89725177delinsAG GRCh37
NC_000010.9:g.89715156_89715157delinsAG NCBI36
NG_007466.2:g.106981_106982delinsAG , LRG_311:g.106981_106982delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1252_1253delinsAG ENSP00000514759.2:p.Pro418Arg
ENST00000710265.1:c.*188_*189delinsAG ENSP00000518161.1:n.*188_*189delinsAG
ENST00000688158.2:n.1894_1895delinsAG
ENST00000688922.2:c.*989_*990delinsAG ENSP00000508742.2:n.*989_*990delinsAG
ENST00000700021.1:c.1114_1115delinsAG ENSP00000514757.1:p.Pro372Arg
ENST00000700022.1:c.*498_*499delinsAG ENSP00000514758.1:n.*498_*499delinsAG
ENST00000700023.1:n.2317_2318delinsAG
ENST00000700024.1:n.2551_2552delinsAG
ENST00000706954.1:c.1159_1160delinsAG ENSP00000516674.1:p.Pro387Arg
ENST00000706955.1:c.*1194_*1195delinsAG ENSP00000516675.1:n.*1194_*1195delinsAG
ENST00000686459.1:c.*745_*746delinsAG ENSP00000508909.1:n.*745_*746delinsAG
ENST00000688158.1:c.*1270_*1271delinsAG ENSP00000509254.1:n.*1270_*1271delinsAG
ENST00000688308.1:c.1159_1160delinsAG ENSP00000508752.1:p.Pro387Arg
ENST00000688922.1:c.1080_1081delinsAG
ENST00000693560.1:c.1678_1679delinsAG ENSP00000509861.1:p.Pro560Arg
ENST00000371953.8:c.1159_1160delinsAG MANE Select ENSP00000361021.3:p.Pro387Arg
ENST00000371953.7:c.1159_1160delinsAG ENSP00000361021.3:p.Pro387Arg
NM_000314.5:c.1159_1160delinsAG NP_000305.3:p.Pro387Arg
NM_000314.6:c.1159_1160delinsAG NP_000305.3:p.Pro387Arg
NM_001304717.2:c.1678_1679delinsAG NP_001291646.2:p.Pro560Arg
NM_001304718.1:c.568_569delinsAG NP_001291647.1:p.Pro190Arg
XM_006717926.2:c.1114_1115delinsAG XP_006717989.1:p.Pro372Arg
XM_011539982.1:c.1063_1064delinsAG XP_011538284.1:p.Pro355Arg
XR_945791.1:n.1729_1730delinsAG
NM_000314.7:c.1159_1160delinsAG NP_000305.3:p.Pro387Arg
NM_001304717.5:c.1678_1679delinsAG NP_001291646.4:p.Pro560Arg
NM_001304718.2:c.568_569delinsAG NP_001291647.1:p.Pro190Arg
NM_000314.8:c.1159_1160delinsAG MANE Select NP_000305.3:p.Pro387Arg