Canonical Allele Identifier: CA891839962
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957981_87957983delinsTAT , CM000672.2:g.87957981_87957983delinsTAT GRCh38
NC_000010.10:g.89717738_89717740delinsTAT , CM000672.1:g.89717738_89717740delinsTAT GRCh37
NC_000010.9:g.89707718_89707720delinsTAT NCBI36
NG_007466.2:g.99543_99545delinsTAT , LRG_311:g.99543_99545delinsTAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.763_765delinsTAT ENSP00000514759.2:p.Val255Tyr
ENST00000710265.1:c.763_765delinsTAT ENSP00000518161.1:p.Val255Tyr
ENST00000472832.3:c.763_765delinsTAT ENSP00000483066.2:p.Val255Tyr
ENST00000688158.2:n.1498_1500delinsTAT
ENST00000688922.2:c.*593_*595delinsTAT ENSP00000508742.2:n.*593_*595delinsTAT
ENST00000700021.1:c.718_720delinsTAT ENSP00000514757.1:p.Val240Tyr
ENST00000700022.1:c.*102_*104delinsTAT ENSP00000514758.1:n.*102_*104delinsTAT
ENST00000700023.1:n.1921_1923delinsTAT
ENST00000700024.1:n.2155_2157delinsTAT
ENST00000700025.1:n.1532_1534delinsTAT
ENST00000700026.1:n.400_402delinsTAT
ENST00000700029.1:c.597_599delinsTAT
ENST00000706954.1:c.763_765delinsTAT ENSP00000516674.1:p.Val255Tyr
ENST00000706955.1:c.*798_*800delinsTAT ENSP00000516675.1:n.*798_*800delinsTAT
ENST00000686459.1:c.*349_*351delinsTAT ENSP00000508909.1:n.*349_*351delinsTAT
ENST00000688158.1:c.*874_*876delinsTAT ENSP00000509254.1:n.*874_*876delinsTAT
ENST00000688308.1:c.763_765delinsTAT ENSP00000508752.1:p.Val255Tyr
ENST00000688922.1:c.684_686delinsTAT
ENST00000693560.1:c.1282_1284delinsTAT ENSP00000509861.1:p.Val428Tyr
ENST00000371953.8:c.763_765delinsTAT MANE Select ENSP00000361021.3:p.Val255Tyr
ENST00000371953.7:c.763_765delinsTAT ENSP00000361021.3:p.Val255Tyr
ENST00000472832.2:c.190_192delinsTAT ENSP00000483066.1:p.Val64Tyr
NM_000314.5:c.763_765delinsTAT NP_000305.3:p.Val255Tyr
NM_000314.6:c.763_765delinsTAT NP_000305.3:p.Val255Tyr
NM_001304717.2:c.1282_1284delinsTAT NP_001291646.2:p.Val428Tyr
NM_001304718.1:c.172_174delinsTAT NP_001291647.1:p.Val58Tyr
XM_006717926.2:c.718_720delinsTAT XP_006717989.1:p.Val240Tyr
XM_011539981.1:c.763_765delinsTAT XP_011538283.1:p.Val255Tyr
XM_011539982.1:c.667_669delinsTAT XP_011538284.1:p.Val223Tyr
XR_945791.1:n.1333_1335delinsTAT
NM_000314.7:c.763_765delinsTAT NP_000305.3:p.Val255Tyr
NM_001304717.5:c.1282_1284delinsTAT NP_001291646.4:p.Val428Tyr
NM_001304718.2:c.172_174delinsTAT NP_001291647.1:p.Val58Tyr
NM_000314.8:c.763_765delinsTAT MANE Select NP_000305.3:p.Val255Tyr