Canonical Allele Identifier: CA891840790
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957948_87957950delinsATG , CM000672.2:g.87957948_87957950delinsATG GRCh38
NC_000010.10:g.89717705_89717707delinsATG , CM000672.1:g.89717705_89717707delinsATG GRCh37
NC_000010.9:g.89707685_89707687delinsATG NCBI36
NG_007466.2:g.99510_99512delinsATG , LRG_311:g.99510_99512delinsATG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.730_732delinsATG ENSP00000514759.2:p.Pro244Met
ENST00000710265.1:c.730_732delinsATG ENSP00000518161.1:p.Pro244Met
ENST00000472832.3:c.730_732delinsATG ENSP00000483066.2:p.Pro244Met
ENST00000688158.2:n.1465_1467delinsATG
ENST00000688922.2:c.*560_*562delinsATG ENSP00000508742.2:n.*560_*562delinsATG
ENST00000700021.1:c.685_687delinsATG ENSP00000514757.1:p.Pro229Met
ENST00000700022.1:c.*69_*71delinsATG ENSP00000514758.1:n.*69_*71delinsATG
ENST00000700023.1:n.1888_1890delinsATG
ENST00000700024.1:n.2122_2124delinsATG
ENST00000700025.1:n.1499_1501delinsATG
ENST00000700026.1:n.367_369delinsATG
ENST00000700029.1:c.564_566delinsATG
ENST00000706954.1:c.730_732delinsATG ENSP00000516674.1:p.Pro244Met
ENST00000706955.1:c.*765_*767delinsATG ENSP00000516675.1:n.*765_*767delinsATG
ENST00000686459.1:c.*316_*318delinsATG ENSP00000508909.1:n.*316_*318delinsATG
ENST00000688158.1:c.*841_*843delinsATG ENSP00000509254.1:n.*841_*843delinsATG
ENST00000688308.1:c.730_732delinsATG ENSP00000508752.1:p.Pro244Met
ENST00000688922.1:c.651_653delinsATG
ENST00000693560.1:c.1249_1251delinsATG ENSP00000509861.1:p.Pro417Met
ENST00000371953.8:c.730_732delinsATG MANE Select ENSP00000361021.3:p.Pro244Met
ENST00000371953.7:c.730_732delinsATG ENSP00000361021.3:p.Pro244Met
ENST00000472832.2:c.157_159delinsATG ENSP00000483066.1:p.Pro53Met
NM_000314.5:c.730_732delinsATG NP_000305.3:p.Pro244Met
NM_000314.6:c.730_732delinsATG NP_000305.3:p.Pro244Met
NM_001304717.2:c.1249_1251delinsATG NP_001291646.2:p.Pro417Met
NM_001304718.1:c.139_141delinsATG NP_001291647.1:p.Pro47Met
XM_006717926.2:c.685_687delinsATG XP_006717989.1:p.Pro229Met
XM_011539981.1:c.730_732delinsATG XP_011538283.1:p.Pro244Met
XM_011539982.1:c.634_636delinsATG XP_011538284.1:p.Pro212Met
XR_945791.1:n.1300_1302delinsATG
NM_000314.7:c.730_732delinsATG NP_000305.3:p.Pro244Met
NM_001304717.5:c.1249_1251delinsATG NP_001291646.4:p.Pro417Met
NM_001304718.2:c.139_141delinsATG NP_001291647.1:p.Pro47Met
NM_000314.8:c.730_732delinsATG MANE Select NP_000305.3:p.Pro244Met