Canonical Allele Identifier: CA470882596
Gene: PTEN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87925519_87925520insT , CM000672.2:g.87925519_87925520insT GRCh38
NC_000010.10:g.89685276_89685277insT , CM000672.1:g.89685276_89685277insT GRCh37
NC_000010.9:g.89675256_89675257insT NCBI36
NG_007466.2:g.67081_67082insT , LRG_311:g.67081_67082insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.171_172insT ENSP00000514759.2:p.Asp58Ter
ENST00000710265.1:c.171_172insT ENSP00000518161.1:p.Asp58Ter
ENST00000472832.3:c.171_172insT ENSP00000483066.2:p.Asp58Ter
ENST00000688158.2:n.906_907insT
ENST00000688922.2:c.171_172insT ENSP00000508742.2:p.Asp58Ter
ENST00000700021.1:c.165-5527_165-5526insT ENSP00000514757.1:n.165-5527_165-5526insT
ENST00000700022.1:c.171_172insT ENSP00000514758.1:p.Asp58Ter
ENST00000700029.1:c.5_6insT
ENST00000706954.1:c.171_172insT ENSP00000516674.1:p.Asp58Ter
ENST00000706955.1:c.*206_*207insT ENSP00000516675.1:n.*206_*207insT
ENST00000686459.1:c.171_172insT ENSP00000508909.1:p.Asp58Ter
ENST00000688158.1:c.*282_*283insT ENSP00000509254.1:n.*282_*283insT
ENST00000688308.1:c.171_172insT ENSP00000508752.1:p.Asp58Ter
ENST00000688922.1:c.40_41insT
ENST00000693560.1:c.690_691insT ENSP00000509861.1:p.Asp231Ter
ENST00000371953.8:c.171_172insT MANE Select ENSP00000361021.3:p.Asp58Ter
ENST00000371953.7:c.171_172insT ENSP00000361021.3:p.Asp58Ter
ENST00000610634.1:c.69_70insT ENSP00000477517.1:p.Asp24Ter
NM_000314.5:c.171_172insT NP_000305.3:p.Asp58Ter
NM_000314.6:c.171_172insT NP_000305.3:p.Asp58Ter
NM_001304717.2:c.690_691insT NP_001291646.2:p.Asp231Ter
NM_001304718.1:c.-541-5527_-541-5526insT NP_001291647.1:n.-541-5527_-541-5526insT
XM_006717926.2:c.165-5527_165-5526insT XP_006717989.1:n.165-5527_165-5526insT
XM_011539981.1:c.171_172insT XP_011538283.1:p.Asp58Ter
XM_011539982.1:c.75_76insT XP_011538284.1:p.Asp26Ter
XR_945789.1:n.883_884insT
XR_945790.1:n.883_884insT
XR_945791.1:n.883_884insT
NM_000314.7:c.171_172insT NP_000305.3:p.Asp58Ter
NM_001304717.5:c.690_691insT NP_001291646.4:p.Asp231Ter
NM_001304718.2:c.-541-5527_-541-5526insT NP_001291647.1:n.-541-5527_-541-5526insT
NM_000314.8:c.171_172insT MANE Select NP_000305.3:p.Asp58Ter