Canonical Allele Identifier: CA891838074
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965431_87965433delinsATG , CM000672.2:g.87965431_87965433delinsATG GRCh38
NC_000010.10:g.89725188_89725190delinsATG , CM000672.1:g.89725188_89725190delinsATG GRCh37
NC_000010.9:g.89715168_89715170delinsATG NCBI36
NG_007466.2:g.106993_106995delinsATG , LRG_311:g.106993_106995delinsATG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1264_1266delinsATG ENSP00000514759.2:p.Pro422Met
ENST00000710265.1:c.*200_*202delinsATG ENSP00000518161.1:n.*200_*202delinsATG
ENST00000688158.2:n.1906_1908delinsATG
ENST00000688922.2:c.*1001_*1003delinsATG ENSP00000508742.2:n.*1001_*1003delinsATG
ENST00000700021.1:c.1126_1128delinsATG ENSP00000514757.1:p.Pro376Met
ENST00000700022.1:c.*510_*512delinsATG ENSP00000514758.1:n.*510_*512delinsATG
ENST00000700023.1:n.2329_2331delinsATG
ENST00000700024.1:n.2563_2565delinsATG
ENST00000706954.1:c.1171_1173delinsATG ENSP00000516674.1:p.Pro391Met
ENST00000706955.1:c.*1206_*1208delinsATG ENSP00000516675.1:n.*1206_*1208delinsATG
ENST00000686459.1:c.*757_*759delinsATG ENSP00000508909.1:n.*757_*759delinsATG
ENST00000688158.1:c.*1282_*1284delinsATG ENSP00000509254.1:n.*1282_*1284delinsATG
ENST00000688308.1:c.1171_1173delinsATG ENSP00000508752.1:p.Pro391Met
ENST00000688922.1:c.1092_1094delinsATG
ENST00000693560.1:c.1690_1692delinsATG ENSP00000509861.1:p.Pro564Met
ENST00000371953.8:c.1171_1173delinsATG MANE Select ENSP00000361021.3:p.Pro391Met
ENST00000371953.7:c.1171_1173delinsATG ENSP00000361021.3:p.Pro391Met
NM_000314.5:c.1171_1173delinsATG NP_000305.3:p.Pro391Met
NM_000314.6:c.1171_1173delinsATG NP_000305.3:p.Pro391Met
NM_001304717.2:c.1690_1692delinsATG NP_001291646.2:p.Pro564Met
NM_001304718.1:c.580_582delinsATG NP_001291647.1:p.Pro194Met
XM_006717926.2:c.1126_1128delinsATG XP_006717989.1:p.Pro376Met
XM_011539982.1:c.1075_1077delinsATG XP_011538284.1:p.Pro359Met
XR_945791.1:n.1741_1743delinsATG
NM_000314.7:c.1171_1173delinsATG NP_000305.3:p.Pro391Met
NM_001304717.5:c.1690_1692delinsATG NP_001291646.4:p.Pro564Met
NM_001304718.2:c.580_582delinsATG NP_001291647.1:p.Pro194Met
NM_000314.8:c.1171_1173delinsATG MANE Select NP_000305.3:p.Pro391Met