Canonical Allele Identifier: CA891837704
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965381_87965382delinsAA , CM000672.2:g.87965381_87965382delinsAA GRCh38
NC_000010.10:g.89725138_89725139delinsAA , CM000672.1:g.89725138_89725139delinsAA GRCh37
NC_000010.9:g.89715118_89715119delinsAA NCBI36
NG_007466.2:g.106943_106944delinsAA , LRG_311:g.106943_106944delinsAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1214_1215delinsAA ENSP00000514759.2:p.Pro405Gln
ENST00000710265.1:c.*150_*151delinsAA ENSP00000518161.1:n.*150_*151delinsAA
ENST00000688158.2:n.1856_1857delinsAA
ENST00000688922.2:c.*951_*952delinsAA ENSP00000508742.2:n.*951_*952delinsAA
ENST00000700021.1:c.1076_1077delinsAA ENSP00000514757.1:p.Pro359Gln
ENST00000700022.1:c.*460_*461delinsAA ENSP00000514758.1:n.*460_*461delinsAA
ENST00000700023.1:n.2279_2280delinsAA
ENST00000700024.1:n.2513_2514delinsAA
ENST00000706954.1:c.1121_1122delinsAA ENSP00000516674.1:p.Pro374Gln
ENST00000706955.1:c.*1156_*1157delinsAA ENSP00000516675.1:n.*1156_*1157delinsAA
ENST00000686459.1:c.*707_*708delinsAA ENSP00000508909.1:n.*707_*708delinsAA
ENST00000688158.1:c.*1232_*1233delinsAA ENSP00000509254.1:n.*1232_*1233delinsAA
ENST00000688308.1:c.1121_1122delinsAA ENSP00000508752.1:p.Pro374Gln
ENST00000688922.1:c.1042_1043delinsAA
ENST00000693560.1:c.1640_1641delinsAA ENSP00000509861.1:p.Pro547Gln
ENST00000371953.8:c.1121_1122delinsAA MANE Select ENSP00000361021.3:p.Pro374Gln
ENST00000371953.7:c.1121_1122delinsAA ENSP00000361021.3:p.Pro374Gln
NM_000314.5:c.1121_1122delinsAA NP_000305.3:p.Pro374Gln
NM_000314.6:c.1121_1122delinsAA NP_000305.3:p.Pro374Gln
NM_001304717.2:c.1640_1641delinsAA NP_001291646.2:p.Pro547Gln
NM_001304718.1:c.530_531delinsAA NP_001291647.1:p.Pro177Gln
XM_006717926.2:c.1076_1077delinsAA XP_006717989.1:p.Pro359Gln
XM_011539982.1:c.1025_1026delinsAA XP_011538284.1:p.Pro342Gln
XR_945791.1:n.1691_1692delinsAA
NM_000314.7:c.1121_1122delinsAA NP_000305.3:p.Pro374Gln
NM_001304717.5:c.1640_1641delinsAA NP_001291646.4:p.Pro547Gln
NM_001304718.2:c.530_531delinsAA NP_001291647.1:p.Pro177Gln
NM_000314.8:c.1121_1122delinsAA MANE Select NP_000305.3:p.Pro374Gln