Canonical Allele Identifier: CA891839953
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957981_87957982delinsCC , CM000672.2:g.87957981_87957982delinsCC GRCh38
NC_000010.10:g.89717738_89717739delinsCC , CM000672.1:g.89717738_89717739delinsCC GRCh37
NC_000010.9:g.89707718_89707719delinsCC NCBI36
NG_007466.2:g.99543_99544delinsCC , LRG_311:g.99543_99544delinsCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.763_764delinsCC ENSP00000514759.2:p.Val255Pro
ENST00000710265.1:c.763_764delinsCC ENSP00000518161.1:p.Val255Pro
ENST00000472832.3:c.763_764delinsCC ENSP00000483066.2:p.Val255Pro
ENST00000688158.2:n.1498_1499delinsCC
ENST00000688922.2:c.*593_*594delinsCC ENSP00000508742.2:n.*593_*594delinsCC
ENST00000700021.1:c.718_719delinsCC ENSP00000514757.1:p.Val240Pro
ENST00000700022.1:c.*102_*103delinsCC ENSP00000514758.1:n.*102_*103delinsCC
ENST00000700023.1:n.1921_1922delinsCC
ENST00000700024.1:n.2155_2156delinsCC
ENST00000700025.1:n.1532_1533delinsCC
ENST00000700026.1:n.400_401delinsCC
ENST00000700029.1:c.597_598delinsCC
ENST00000706954.1:c.763_764delinsCC ENSP00000516674.1:p.Val255Pro
ENST00000706955.1:c.*798_*799delinsCC ENSP00000516675.1:n.*798_*799delinsCC
ENST00000686459.1:c.*349_*350delinsCC ENSP00000508909.1:n.*349_*350delinsCC
ENST00000688158.1:c.*874_*875delinsCC ENSP00000509254.1:n.*874_*875delinsCC
ENST00000688308.1:c.763_764delinsCC ENSP00000508752.1:p.Val255Pro
ENST00000688922.1:c.684_685delinsCC
ENST00000693560.1:c.1282_1283delinsCC ENSP00000509861.1:p.Val428Pro
ENST00000371953.8:c.763_764delinsCC MANE Select ENSP00000361021.3:p.Val255Pro
ENST00000371953.7:c.763_764delinsCC ENSP00000361021.3:p.Val255Pro
ENST00000472832.2:c.190_191delinsCC ENSP00000483066.1:p.Val64Pro
NM_000314.5:c.763_764delinsCC NP_000305.3:p.Val255Pro
NM_000314.6:c.763_764delinsCC NP_000305.3:p.Val255Pro
NM_001304717.2:c.1282_1283delinsCC NP_001291646.2:p.Val428Pro
NM_001304718.1:c.172_173delinsCC NP_001291647.1:p.Val58Pro
XM_006717926.2:c.718_719delinsCC XP_006717989.1:p.Val240Pro
XM_011539981.1:c.763_764delinsCC XP_011538283.1:p.Val255Pro
XM_011539982.1:c.667_668delinsCC XP_011538284.1:p.Val223Pro
XR_945791.1:n.1333_1334delinsCC
NM_000314.7:c.763_764delinsCC NP_000305.3:p.Val255Pro
NM_001304717.5:c.1282_1283delinsCC NP_001291646.4:p.Val428Pro
NM_001304718.2:c.172_173delinsCC NP_001291647.1:p.Val58Pro
NM_000314.8:c.763_764delinsCC MANE Select NP_000305.3:p.Val255Pro