Canonical Allele Identifier: CA1926142796

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863224_87863225delinsTG , CM000672.2:g.87863224_87863225delinsTG GRCh38
NC_000010.10:g.89622981_89622982delinsTG , CM000672.1:g.89622981_89622982delinsTG GRCh37
NC_000010.9:g.89612961_89612962delinsTG NCBI36
NG_007466.2:g.4787_4788delinsTG , LRG_311:g.4787_4788delinsTG
NG_033079.1:g.5213_5214delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+582_-17+583delinsTG (PTEN) ENSP00000516674.1:n.-17+582_-17+583delinsTG
ENST00000688308.1:c.-17+111_-17+112delinsTG (PTEN) ENSP00000508752.1:n.-17+111_-17+112delinsTG
ENST00000445946.5:c.-738_-737delinsCA (KLLN) MANE Select ENSP00000392204.2:n.-738_-737delinsCA
ENST00000371953.7:c.-1246_-1245delinsTG (PTEN) ENSP00000361021.3:n.-1246_-1245delinsTG
ENST00000445946.3:c.-738_-737delinsCA (KLLN) ENSP00000392204.2:n.-738_-737delinsCA
NM_001126049.1:c.-738_-737delinsCA (KLLN) NP_001119521.1:n.-738_-737delinsCA
NM_001126049.2:c.-738_-737delinsCA (KLLN) MANE Select NP_001119521.1:n.-738_-737delinsCA