Canonical Allele Identifier: CA1926142933

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863375_87863401delinsACTCTGCGCTCGCACCCAGAGCTACCG , CM000672.2:g.87863375_87863401delinsACTCTGCGCTCGCACCCAGAGCTACCG GRCh38
NC_000010.10:g.89623132_89623158delinsACTCTGCGCTCGCACCCAGAGCTACCG , CM000672.1:g.89623132_89623158delinsACTCTGCGCTCGCACCCAGAGCTACCG GRCh37
NC_000010.9:g.89613112_89613138delinsACTCTGCGCTCGCACCCAGAGCTACCG NCBI36
NG_007466.2:g.4938_4964delinsACTCTGCGCTCGCACCCAGAGCTACCG , LRG_311:g.4938_4964delinsACTCTGCGCTCGCACCCAGAGCTACCG
NG_033079.1:g.5037_5063delinsCGGTAGCTCTGGGTGCGAGCGCAGAGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+733_-17+759delinsACTCTGCGCTCGCACCCAGAGCTACCG (PTEN) ENSP00000516674.1:n.-17+733_-17+759delinsACTCTGCGCTCGCACCCAGA...
ENST00000688308.1:c.-17+262_-17+288delinsACTCTGCGCTCGCACCCAGAGCTACCG (PTEN) ENSP00000508752.1:n.-17+262_-17+288delinsACTCTGCGCTCGCACCCAGA...
ENST00000445946.5:c.-914_-888delinsCGGTAGCTCTGGGTGCGAGCGCAGAGT (KLLN) MANE Select ENSP00000392204.2:n.-914_-888delinsCGGTAGCTCTGGGTGCGAGCGCAGAG...
ENST00000371953.7:c.-1095_-1069delinsACTCTGCGCTCGCACCCAGAGCTACCG (PTEN) ENSP00000361021.3:n.-1095_-1069delinsACTCTGCGCTCGCACCCAGAGCTA...
ENST00000445946.3:c.-914_-888delinsCGGTAGCTCTGGGTGCGAGCGCAGAGT (KLLN) ENSP00000392204.2:n.-914_-888delinsCGGTAGCTCTGGGTGCGAGCGCAGAG...
NM_001126049.1:c.-914_-888delinsCGGTAGCTCTGGGTGCGAGCGCAGAGT (KLLN) NP_001119521.1:n.-914_-888delinsCGGTAGCTCTGGGTGCGAGCGCAGAGT
NM_001126049.2:c.-914_-888delinsCGGTAGCTCTGGGTGCGAGCGCAGAGT (KLLN) MANE Select NP_001119521.1:n.-914_-888delinsCGGTAGCTCTGGGTGCGAGCGCAGAGT