Canonical Allele Identifier: CA891839793
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957948_87957950delinsTGG , CM000672.2:g.87957948_87957950delinsTGG GRCh38
NC_000010.10:g.89717705_89717707delinsTGG , CM000672.1:g.89717705_89717707delinsTGG GRCh37
NC_000010.9:g.89707685_89707687delinsTGG NCBI36
NG_007466.2:g.99510_99512delinsTGG , LRG_311:g.99510_99512delinsTGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.730_732delinsTGG ENSP00000514759.2:p.Pro244Trp
ENST00000710265.1:c.730_732delinsTGG ENSP00000518161.1:p.Pro244Trp
ENST00000472832.3:c.730_732delinsTGG ENSP00000483066.2:p.Pro244Trp
ENST00000688158.2:n.1465_1467delinsTGG
ENST00000688922.2:c.*560_*562delinsTGG ENSP00000508742.2:n.*560_*562delinsTGG
ENST00000700021.1:c.685_687delinsTGG ENSP00000514757.1:p.Pro229Trp
ENST00000700022.1:c.*69_*71delinsTGG ENSP00000514758.1:n.*69_*71delinsTGG
ENST00000700023.1:n.1888_1890delinsTGG
ENST00000700024.1:n.2122_2124delinsTGG
ENST00000700025.1:n.1499_1501delinsTGG
ENST00000700026.1:n.367_369delinsTGG
ENST00000700029.1:c.564_566delinsTGG
ENST00000706954.1:c.730_732delinsTGG ENSP00000516674.1:p.Pro244Trp
ENST00000706955.1:c.*765_*767delinsTGG ENSP00000516675.1:n.*765_*767delinsTGG
ENST00000686459.1:c.*316_*318delinsTGG ENSP00000508909.1:n.*316_*318delinsTGG
ENST00000688158.1:c.*841_*843delinsTGG ENSP00000509254.1:n.*841_*843delinsTGG
ENST00000688308.1:c.730_732delinsTGG ENSP00000508752.1:p.Pro244Trp
ENST00000688922.1:c.651_653delinsTGG
ENST00000693560.1:c.1249_1251delinsTGG ENSP00000509861.1:p.Pro417Trp
ENST00000371953.8:c.730_732delinsTGG MANE Select ENSP00000361021.3:p.Pro244Trp
ENST00000371953.7:c.730_732delinsTGG ENSP00000361021.3:p.Pro244Trp
ENST00000472832.2:c.157_159delinsTGG ENSP00000483066.1:p.Pro53Trp
NM_000314.5:c.730_732delinsTGG NP_000305.3:p.Pro244Trp
NM_000314.6:c.730_732delinsTGG NP_000305.3:p.Pro244Trp
NM_001304717.2:c.1249_1251delinsTGG NP_001291646.2:p.Pro417Trp
NM_001304718.1:c.139_141delinsTGG NP_001291647.1:p.Pro47Trp
XM_006717926.2:c.685_687delinsTGG XP_006717989.1:p.Pro229Trp
XM_011539981.1:c.730_732delinsTGG XP_011538283.1:p.Pro244Trp
XM_011539982.1:c.634_636delinsTGG XP_011538284.1:p.Pro212Trp
XR_945791.1:n.1300_1302delinsTGG
NM_000314.7:c.730_732delinsTGG NP_000305.3:p.Pro244Trp
NM_001304717.5:c.1249_1251delinsTGG NP_001291646.4:p.Pro417Trp
NM_001304718.2:c.139_141delinsTGG NP_001291647.1:p.Pro47Trp
NM_000314.8:c.730_732delinsTGG MANE Select NP_000305.3:p.Pro244Trp