Canonical Allele Identifier: CA645558978
Gene: PTEN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87864511_87864513del , CM000672.2:g.87864511_87864513del GRCh38
NC_000010.10:g.89624268_89624270del , CM000672.1:g.89624268_89624270del GRCh37
NC_000010.9:g.89614248_89614250del NCBI36
NG_007466.2:g.6073_6075del , LRG_311:g.6073_6075del
NG_033079.1:g.3927_3929del

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.42_44del ENSP00000514759.2:p.Arg15del
ENST00000710265.1:c.42_44del ENSP00000518161.1:p.Arg15del
ENST00000472832.3:c.42_44del ENSP00000483066.2:p.Arg15del
ENST00000688922.2:c.42_44del ENSP00000508742.2:p.Arg15del
ENST00000700021.1:c.42_44del ENSP00000514757.1:p.Arg15del
ENST00000700022.1:c.42_44del ENSP00000514758.1:p.Arg15del
ENST00000706954.1:c.42_44del ENSP00000516674.1:p.Arg15del
ENST00000706955.1:c.42_44del ENSP00000516675.1:p.Arg15del
ENST00000686459.1:c.42_44del ENSP00000508909.1:p.Arg15del
ENST00000688158.1:c.42_44del ENSP00000509254.1:p.Arg15del
ENST00000688308.1:c.42_44del ENSP00000508752.1:p.Arg15del
ENST00000693560.1:c.561_563del ENSP00000509861.1:p.Arg188del
ENST00000371953.8:c.42_44del MANE Select ENSP00000361021.3:p.Arg15del
ENST00000371953.7:c.42_44del ENSP00000361021.3:p.Arg15del
ENST00000462694.1:n.44_46del
ENST00000487939.1:n.63_65del
ENST00000610634.1:c.-61_-59del ENSP00000477517.1:n.-61_-59del
ENST00000618586.1:n.11_13del
NM_000314.5:c.42_44del NP_000305.3:p.Arg15del
NM_000314.6:c.42_44del NP_000305.3:p.Arg15del
NM_001304717.2:c.561_563del NP_001291646.2:p.Arg188del
NM_001304718.1:c.-664_-662del NP_001291647.1:n.-664_-662del
XM_006717926.2:c.42_44del XP_006717989.1:p.Arg15del
XM_011539981.1:c.42_44del XP_011538283.1:p.Arg15del
XR_945789.1:n.754_756del
XR_945790.1:n.754_756del
XR_945791.1:n.754_756del
NM_000314.7:c.42_44del NP_000305.3:p.Arg15del
NM_001304717.5:c.561_563del NP_001291646.4:p.Arg188del
NM_001304718.2:c.-664_-662del NP_001291647.1:n.-664_-662del
NM_000314.8:c.42_44del MANE Select NP_000305.3:p.Arg15del