Canonical Allele Identifier: CA891834636
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87894048_87894050delinsTAA , CM000672.2:g.87894048_87894050delinsTAA GRCh38
NC_000010.10:g.89653805_89653807delinsTAA , CM000672.1:g.89653805_89653807delinsTAA GRCh37
NC_000010.9:g.89643785_89643787delinsTAA NCBI36
NG_007466.2:g.35610_35612delinsTAA , LRG_311:g.35610_35612delinsTAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.103_105delinsTAA ENSP00000514759.2:p.Met35Ter
ENST00000710265.1:c.103_105delinsTAA ENSP00000518161.1:p.Met35Ter
ENST00000472832.3:c.103_105delinsTAA ENSP00000483066.2:p.Met35Ter
ENST00000688158.2:n.899+13610_899+13612delinsTAA
ENST00000688922.2:c.103_105delinsTAA ENSP00000508742.2:p.Met35Ter
ENST00000700021.1:c.103_105delinsTAA ENSP00000514757.1:p.Met35Ter
ENST00000700022.1:c.103_105delinsTAA ENSP00000514758.1:p.Met35Ter
ENST00000706954.1:c.103_105delinsTAA ENSP00000516674.1:p.Met35Ter
ENST00000706955.1:c.*138_*140delinsTAA ENSP00000516675.1:n.*138_*140delinsTAA
ENST00000686459.1:c.103_105delinsTAA ENSP00000508909.1:p.Met35Ter
ENST00000688158.1:c.*275+13610_*275+13612delinsTAA ENSP00000509254.1:n.*275+13610_*275+13612delinsTAA
ENST00000688308.1:c.103_105delinsTAA ENSP00000508752.1:p.Met35Ter
ENST00000693560.1:c.622_624delinsTAA ENSP00000509861.1:p.Met208Ter
ENST00000371953.8:c.103_105delinsTAA MANE Select ENSP00000361021.3:p.Met35Ter
ENST00000371953.7:c.103_105delinsTAA ENSP00000361021.3:p.Met35Ter
ENST00000462694.1:n.105_107delinsTAA
ENST00000610634.1:c.1_3delinsTAA ENSP00000477517.1:p.Met1Ter
NM_000314.5:c.103_105delinsTAA NP_000305.3:p.Met35Ter
NM_000314.6:c.103_105delinsTAA NP_000305.3:p.Met35Ter
NM_001304717.2:c.622_624delinsTAA NP_001291646.2:p.Met208Ter
NM_001304718.1:c.-603_-601delinsTAA NP_001291647.1:n.-603_-601delinsTAA
XM_006717926.2:c.103_105delinsTAA XP_006717989.1:p.Met35Ter
XM_011539981.1:c.103_105delinsTAA XP_011538283.1:p.Met35Ter
XM_011539982.1:c.68+13610_68+13612delinsTAA XP_011538284.1:n.68+13610_68+13612delinsTAA
XR_945789.1:n.815_817delinsTAA
XR_945790.1:n.815_817delinsTAA
XR_945791.1:n.815_817delinsTAA
NM_000314.7:c.103_105delinsTAA NP_000305.3:p.Met35Ter
NM_001304717.5:c.622_624delinsTAA NP_001291646.4:p.Met208Ter
NM_001304718.2:c.-603_-601delinsTAA NP_001291647.1:n.-603_-601delinsTAA
NM_000314.8:c.103_105delinsTAA MANE Select NP_000305.3:p.Met35Ter