Canonical Allele Identifier: CA891835177
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87894078_87894079delinsTA , CM000672.2:g.87894078_87894079delinsTA GRCh38
NC_000010.10:g.89653835_89653836delinsTA , CM000672.1:g.89653835_89653836delinsTA GRCh37
NC_000010.9:g.89643815_89643816delinsTA NCBI36
NG_007466.2:g.35640_35641delinsTA , LRG_311:g.35640_35641delinsTA

Transcript Alleles

HGVS Amino-acid change
ENST00000700029.2:c.133_134delinsTA ENSP00000514759.2:p.Val45Ter
ENST00000710265.1:c.133_134delinsTA ENSP00000518161.1:p.Val45Ter
ENST00000472832.3:c.133_134delinsTA ENSP00000483066.2:p.Val45Ter
ENST00000688158.2:n.899+13640_899+13641delinsTA
ENST00000688922.2:c.133_134delinsTA ENSP00000508742.2:p.Val45Ter
ENST00000700021.1:c.133_134delinsTA ENSP00000514757.1:p.Val45Ter
ENST00000700022.1:c.133_134delinsTA ENSP00000514758.1:p.Val45Ter
ENST00000706954.1:c.133_134delinsTA ENSP00000516674.1:p.Val45Ter
ENST00000706955.1:c.*168_*169delinsTA ENSP00000516675.1:n.*168_*169delinsTA
ENST00000686459.1:c.133_134delinsTA ENSP00000508909.1:p.Val45Ter
ENST00000688158.1:c.*275+13640_*275+13641delinsTA ENSP00000509254.1:n.*275+13640_*275+13641delinsTA
ENST00000688308.1:c.133_134delinsTA ENSP00000508752.1:p.Val45Ter
ENST00000688922.1:c.2_3delinsTA
ENST00000693560.1:c.652_653delinsTA ENSP00000509861.1:p.Val218Ter
ENST00000371953.8:c.133_134delinsTA MANE Select ENSP00000361021.3:p.Val45Ter
ENST00000371953.7:c.133_134delinsTA ENSP00000361021.3:p.Val45Ter
ENST00000462694.1:n.135_136delinsTA
ENST00000610634.1:c.31_32delinsTA ENSP00000477517.1:p.Val11Ter
NM_000314.5:c.133_134delinsTA NP_000305.3:p.Val45Ter
NM_000314.6:c.133_134delinsTA NP_000305.3:p.Val45Ter
NM_001304717.2:c.652_653delinsTA NP_001291646.2:p.Val218Ter
NM_001304718.1:c.-573_-572delinsTA NP_001291647.1:n.-573_-572delinsTA
XM_006717926.2:c.133_134delinsTA XP_006717989.1:p.Val45Ter
XM_011539981.1:c.133_134delinsTA XP_011538283.1:p.Val45Ter
XM_011539982.1:c.68+13640_68+13641delinsTA XP_011538284.1:n.68+13640_68+13641delinsTA
XR_945789.1:n.845_846delinsTA
XR_945790.1:n.845_846delinsTA
XR_945791.1:n.845_846delinsTA
NM_000314.7:c.133_134delinsTA NP_000305.3:p.Val45Ter
NM_001304717.5:c.652_653delinsTA NP_001291646.4:p.Val218Ter
NM_001304718.2:c.-573_-572delinsTA NP_001291647.1:n.-573_-572delinsTA
NM_000314.8:c.133_134delinsTA MANE Select NP_000305.3:p.Val45Ter