Canonical Allele Identifier: CA2579927159
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87864512_87864514del , CM000672.2:g.87864512_87864514del GRCh38
NC_000010.10:g.89624269_89624271del , CM000672.1:g.89624269_89624271del GRCh37
NC_000010.9:g.89614249_89614251del NCBI36
NG_007466.2:g.6074_6076del , LRG_311:g.6074_6076del
NG_033079.1:g.3924_3926del

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.43_45del ENSP00000514759.2:p.Arg15del
ENST00000710265.1:c.43_45del ENSP00000518161.1:p.Arg15del
ENST00000472832.3:c.43_45del ENSP00000483066.2:p.Arg15del
ENST00000688922.2:c.43_45del ENSP00000508742.2:p.Arg15del
ENST00000700021.1:c.43_45del ENSP00000514757.1:p.Arg15del
ENST00000700022.1:c.43_45del ENSP00000514758.1:p.Arg15del
ENST00000706954.1:c.43_45del ENSP00000516674.1:p.Arg15del
ENST00000706955.1:c.43_45del ENSP00000516675.1:p.Arg15del
ENST00000686459.1:c.43_45del ENSP00000508909.1:p.Arg15del
ENST00000688158.1:c.43_45del ENSP00000509254.1:p.Arg15del
ENST00000688308.1:c.43_45del ENSP00000508752.1:p.Arg15del
ENST00000693560.1:c.562_564del ENSP00000509861.1:p.Arg188del
ENST00000371953.8:c.43_45del MANE Select ENSP00000361021.3:p.Arg15del
ENST00000371953.7:c.43_45del ENSP00000361021.3:p.Arg15del
ENST00000462694.1:n.45_47del
ENST00000487939.1:n.64_66del
ENST00000610634.1:c.-60_-58del ENSP00000477517.1:n.-60_-58del
ENST00000618586.1:n.12_14del
NM_000314.5:c.43_45del NP_000305.3:p.Arg15del
NM_000314.6:c.43_45del NP_000305.3:p.Arg15del
NM_001304717.2:c.562_564del NP_001291646.2:p.Arg188del
NM_001304718.1:c.-663_-661del NP_001291647.1:n.-663_-661del
XM_006717926.2:c.43_45del XP_006717989.1:p.Arg15del
XM_011539981.1:c.43_45del XP_011538283.1:p.Arg15del
XR_945789.1:n.755_757del
XR_945790.1:n.755_757del
XR_945791.1:n.755_757del
NM_000314.7:c.43_45del NP_000305.3:p.Arg15del
NM_001304717.5:c.562_564del NP_001291646.4:p.Arg188del
NM_001304718.2:c.-663_-661del NP_001291647.1:n.-663_-661del
NM_000314.8:c.43_45del MANE Select NP_000305.3:p.Arg15del