Canonical Allele Identifier: CA891839964
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957981_87957983delinsTTG , CM000672.2:g.87957981_87957983delinsTTG GRCh38
NC_000010.10:g.89717738_89717740delinsTTG , CM000672.1:g.89717738_89717740delinsTTG GRCh37
NC_000010.9:g.89707718_89707720delinsTTG NCBI36
NG_007466.2:g.99543_99545delinsTTG , LRG_311:g.99543_99545delinsTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.763_765delinsTTG ENSP00000514759.2:p.Val255Leu
ENST00000710265.1:c.763_765delinsTTG ENSP00000518161.1:p.Val255Leu
ENST00000472832.3:c.763_765delinsTTG ENSP00000483066.2:p.Val255Leu
ENST00000688158.2:n.1498_1500delinsTTG
ENST00000688922.2:c.*593_*595delinsTTG ENSP00000508742.2:n.*593_*595delinsTTG
ENST00000700021.1:c.718_720delinsTTG ENSP00000514757.1:p.Val240Leu
ENST00000700022.1:c.*102_*104delinsTTG ENSP00000514758.1:n.*102_*104delinsTTG
ENST00000700023.1:n.1921_1923delinsTTG
ENST00000700024.1:n.2155_2157delinsTTG
ENST00000700025.1:n.1532_1534delinsTTG
ENST00000700026.1:n.400_402delinsTTG
ENST00000700029.1:c.597_599delinsTTG
ENST00000706954.1:c.763_765delinsTTG ENSP00000516674.1:p.Val255Leu
ENST00000706955.1:c.*798_*800delinsTTG ENSP00000516675.1:n.*798_*800delinsTTG
ENST00000686459.1:c.*349_*351delinsTTG ENSP00000508909.1:n.*349_*351delinsTTG
ENST00000688158.1:c.*874_*876delinsTTG ENSP00000509254.1:n.*874_*876delinsTTG
ENST00000688308.1:c.763_765delinsTTG ENSP00000508752.1:p.Val255Leu
ENST00000688922.1:c.684_686delinsTTG
ENST00000693560.1:c.1282_1284delinsTTG ENSP00000509861.1:p.Val428Leu
ENST00000371953.8:c.763_765delinsTTG MANE Select ENSP00000361021.3:p.Val255Leu
ENST00000371953.7:c.763_765delinsTTG ENSP00000361021.3:p.Val255Leu
ENST00000472832.2:c.190_192delinsTTG ENSP00000483066.1:p.Val64Leu
NM_000314.5:c.763_765delinsTTG NP_000305.3:p.Val255Leu
NM_000314.6:c.763_765delinsTTG NP_000305.3:p.Val255Leu
NM_001304717.2:c.1282_1284delinsTTG NP_001291646.2:p.Val428Leu
NM_001304718.1:c.172_174delinsTTG NP_001291647.1:p.Val58Leu
XM_006717926.2:c.718_720delinsTTG XP_006717989.1:p.Val240Leu
XM_011539981.1:c.763_765delinsTTG XP_011538283.1:p.Val255Leu
XM_011539982.1:c.667_669delinsTTG XP_011538284.1:p.Val223Leu
XR_945791.1:n.1333_1335delinsTTG
NM_000314.7:c.763_765delinsTTG NP_000305.3:p.Val255Leu
NM_001304717.5:c.1282_1284delinsTTG NP_001291646.4:p.Val428Leu
NM_001304718.2:c.172_174delinsTTG NP_001291647.1:p.Val58Leu
NM_000314.8:c.763_765delinsTTG MANE Select NP_000305.3:p.Val255Leu