Canonical Allele Identifier: CA891839786
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957948_87957950delinsAGA , CM000672.2:g.87957948_87957950delinsAGA GRCh38
NC_000010.10:g.89717705_89717707delinsAGA , CM000672.1:g.89717705_89717707delinsAGA GRCh37
NC_000010.9:g.89707685_89707687delinsAGA NCBI36
NG_007466.2:g.99510_99512delinsAGA , LRG_311:g.99510_99512delinsAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.730_732delinsAGA ENSP00000514759.2:p.Pro244Arg
ENST00000710265.1:c.730_732delinsAGA ENSP00000518161.1:p.Pro244Arg
ENST00000472832.3:c.730_732delinsAGA ENSP00000483066.2:p.Pro244Arg
ENST00000688158.2:n.1465_1467delinsAGA
ENST00000688922.2:c.*560_*562delinsAGA ENSP00000508742.2:n.*560_*562delinsAGA
ENST00000700021.1:c.685_687delinsAGA ENSP00000514757.1:p.Pro229Arg
ENST00000700022.1:c.*69_*71delinsAGA ENSP00000514758.1:n.*69_*71delinsAGA
ENST00000700023.1:n.1888_1890delinsAGA
ENST00000700024.1:n.2122_2124delinsAGA
ENST00000700025.1:n.1499_1501delinsAGA
ENST00000700026.1:n.367_369delinsAGA
ENST00000700029.1:c.564_566delinsAGA
ENST00000706954.1:c.730_732delinsAGA ENSP00000516674.1:p.Pro244Arg
ENST00000706955.1:c.*765_*767delinsAGA ENSP00000516675.1:n.*765_*767delinsAGA
ENST00000686459.1:c.*316_*318delinsAGA ENSP00000508909.1:n.*316_*318delinsAGA
ENST00000688158.1:c.*841_*843delinsAGA ENSP00000509254.1:n.*841_*843delinsAGA
ENST00000688308.1:c.730_732delinsAGA ENSP00000508752.1:p.Pro244Arg
ENST00000688922.1:c.651_653delinsAGA
ENST00000693560.1:c.1249_1251delinsAGA ENSP00000509861.1:p.Pro417Arg
ENST00000371953.8:c.730_732delinsAGA MANE Select ENSP00000361021.3:p.Pro244Arg
ENST00000371953.7:c.730_732delinsAGA ENSP00000361021.3:p.Pro244Arg
ENST00000472832.2:c.157_159delinsAGA ENSP00000483066.1:p.Pro53Arg
NM_000314.5:c.730_732delinsAGA NP_000305.3:p.Pro244Arg
NM_000314.6:c.730_732delinsAGA NP_000305.3:p.Pro244Arg
NM_001304717.2:c.1249_1251delinsAGA NP_001291646.2:p.Pro417Arg
NM_001304718.1:c.139_141delinsAGA NP_001291647.1:p.Pro47Arg
XM_006717926.2:c.685_687delinsAGA XP_006717989.1:p.Pro229Arg
XM_011539981.1:c.730_732delinsAGA XP_011538283.1:p.Pro244Arg
XM_011539982.1:c.634_636delinsAGA XP_011538284.1:p.Pro212Arg
XR_945791.1:n.1300_1302delinsAGA
NM_000314.7:c.730_732delinsAGA NP_000305.3:p.Pro244Arg
NM_001304717.5:c.1249_1251delinsAGA NP_001291646.4:p.Pro417Arg
NM_001304718.2:c.139_141delinsAGA NP_001291647.1:p.Pro47Arg
NM_000314.8:c.730_732delinsAGA MANE Select NP_000305.3:p.Pro244Arg