Canonical Allele Identifier: CA645554047
Gene: PTEN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957967_87957968insGCCCT , CM000672.2:g.87957967_87957968insGCCCT GRCh38
NC_000010.10:g.89717724_89717725insGCCCT , CM000672.1:g.89717724_89717725insGCCCT GRCh37
NC_000010.9:g.89707704_89707705insGCCCT NCBI36
NG_007466.2:g.99529_99530insGCCCT , LRG_311:g.99529_99530insGCCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.749_750insGCCCT ENSP00000514759.2:p.Cys250TrpfsTer8
ENST00000710265.1:c.749_750insGCCCT ENSP00000518161.1:p.Cys250TrpfsTer8
ENST00000472832.3:c.749_750insGCCCT ENSP00000483066.2:p.Cys250TrpfsTer8
ENST00000688158.2:n.1484_1485insGCCCT
ENST00000688922.2:c.*579_*580insGCCCT ENSP00000508742.2:n.*579_*580insGCCCT
ENST00000700021.1:c.704_705insGCCCT ENSP00000514757.1:p.Cys235TrpfsTer8
ENST00000700022.1:c.*88_*89insGCCCT ENSP00000514758.1:n.*88_*89insGCCCT
ENST00000700023.1:n.1907_1908insGCCCT
ENST00000700024.1:n.2141_2142insGCCCT
ENST00000700025.1:n.1518_1519insGCCCT
ENST00000700026.1:n.386_387insGCCCT
ENST00000700029.1:c.583_584insGCCCT
ENST00000706954.1:c.749_750insGCCCT ENSP00000516674.1:p.Cys250TrpfsTer8
ENST00000706955.1:c.*784_*785insGCCCT ENSP00000516675.1:n.*784_*785insGCCCT
ENST00000686459.1:c.*335_*336insGCCCT ENSP00000508909.1:n.*335_*336insGCCCT
ENST00000688158.1:c.*860_*861insGCCCT ENSP00000509254.1:n.*860_*861insGCCCT
ENST00000688308.1:c.749_750insGCCCT ENSP00000508752.1:p.Cys250TrpfsTer8
ENST00000688922.1:c.670_671insGCCCT
ENST00000693560.1:c.1268_1269insGCCCT ENSP00000509861.1:p.Cys423TrpfsTer8
ENST00000371953.8:c.749_750insGCCCT MANE Select ENSP00000361021.3:p.Cys250TrpfsTer8
ENST00000371953.7:c.749_750insGCCCT ENSP00000361021.3:p.Cys250TrpfsTer8
ENST00000472832.2:c.176_177insGCCCT ENSP00000483066.1:p.Cys59TrpfsTer8
NM_000314.5:c.749_750insGCCCT NP_000305.3:p.Cys250TrpfsTer8
NM_000314.6:c.749_750insGCCCT NP_000305.3:p.Cys250TrpfsTer8
NM_001304717.2:c.1268_1269insGCCCT NP_001291646.2:p.Cys423TrpfsTer8
NM_001304718.1:c.158_159insGCCCT NP_001291647.1:p.Cys53TrpfsTer8
XM_006717926.2:c.704_705insGCCCT XP_006717989.1:p.Cys235TrpfsTer8
XM_011539981.1:c.749_750insGCCCT XP_011538283.1:p.Cys250TrpfsTer8
XM_011539982.1:c.653_654insGCCCT XP_011538284.1:p.Cys218TrpfsTer8
XR_945791.1:n.1319_1320insGCCCT
NM_000314.7:c.749_750insGCCCT NP_000305.3:p.Cys250TrpfsTer8
NM_001304717.5:c.1268_1269insGCCCT NP_001291646.4:p.Cys423TrpfsTer8
NM_001304718.2:c.158_159insGCCCT NP_001291647.1:p.Cys53TrpfsTer8
NM_000314.8:c.749_750insGCCCT MANE Select NP_000305.3:p.Cys250TrpfsTer8