Canonical Allele Identifier: CA891837676
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965380_87965382delinsAGA , CM000672.2:g.87965380_87965382delinsAGA GRCh38
NC_000010.10:g.89725137_89725139delinsAGA , CM000672.1:g.89725137_89725139delinsAGA GRCh37
NC_000010.9:g.89715117_89715119delinsAGA NCBI36
NG_007466.2:g.106942_106944delinsAGA , LRG_311:g.106942_106944delinsAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1213_1215delinsAGA ENSP00000514759.2:p.Pro405Arg
ENST00000710265.1:c.*149_*151delinsAGA ENSP00000518161.1:n.*149_*151delinsAGA
ENST00000688158.2:n.1855_1857delinsAGA
ENST00000688922.2:c.*950_*952delinsAGA ENSP00000508742.2:n.*950_*952delinsAGA
ENST00000700021.1:c.1075_1077delinsAGA ENSP00000514757.1:p.Pro359Arg
ENST00000700022.1:c.*459_*461delinsAGA ENSP00000514758.1:n.*459_*461delinsAGA
ENST00000700023.1:n.2278_2280delinsAGA
ENST00000700024.1:n.2512_2514delinsAGA
ENST00000706954.1:c.1120_1122delinsAGA ENSP00000516674.1:p.Pro374Arg
ENST00000706955.1:c.*1155_*1157delinsAGA ENSP00000516675.1:n.*1155_*1157delinsAGA
ENST00000686459.1:c.*706_*708delinsAGA ENSP00000508909.1:n.*706_*708delinsAGA
ENST00000688158.1:c.*1231_*1233delinsAGA ENSP00000509254.1:n.*1231_*1233delinsAGA
ENST00000688308.1:c.1120_1122delinsAGA ENSP00000508752.1:p.Pro374Arg
ENST00000688922.1:c.1041_1043delinsAGA
ENST00000693560.1:c.1639_1641delinsAGA ENSP00000509861.1:p.Pro547Arg
ENST00000371953.8:c.1120_1122delinsAGA MANE Select ENSP00000361021.3:p.Pro374Arg
ENST00000371953.7:c.1120_1122delinsAGA ENSP00000361021.3:p.Pro374Arg
NM_000314.5:c.1120_1122delinsAGA NP_000305.3:p.Pro374Arg
NM_000314.6:c.1120_1122delinsAGA NP_000305.3:p.Pro374Arg
NM_001304717.2:c.1639_1641delinsAGA NP_001291646.2:p.Pro547Arg
NM_001304718.1:c.529_531delinsAGA NP_001291647.1:p.Pro177Arg
XM_006717926.2:c.1075_1077delinsAGA XP_006717989.1:p.Pro359Arg
XM_011539982.1:c.1024_1026delinsAGA XP_011538284.1:p.Pro342Arg
XR_945791.1:n.1690_1692delinsAGA
NM_000314.7:c.1120_1122delinsAGA NP_000305.3:p.Pro374Arg
NM_001304717.5:c.1639_1641delinsAGA NP_001291646.4:p.Pro547Arg
NM_001304718.2:c.529_531delinsAGA NP_001291647.1:p.Pro177Arg
NM_000314.8:c.1120_1122delinsAGA MANE Select NP_000305.3:p.Pro374Arg