Canonical Allele Identifier: CA1926142830
Gene: PTEN HGNC NCBI
KLLN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863269_87863281delinsTGCAAAAGCCGCA , CM000672.2:g.87863269_87863281delinsTGCAAAAGCCGCA GRCh38
NC_000010.10:g.89623026_89623038delinsTGCAAAAGCCGCA , CM000672.1:g.89623026_89623038delinsTGCAAAAGCCGCA GRCh37
NC_000010.9:g.89613006_89613018delinsTGCAAAAGCCGCA NCBI36
NG_007466.2:g.4832_4844delinsTGCAAAAGCCGCA , LRG_311:g.4832_4844delinsTGCAAAAGCCGCA
NG_033079.1:g.5157_5169delinsTGCGGCTTTTGCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+627_-17+639delinsTGCAAAAGCCGCA (PTEN) ENSP00000516674.1:n.-17+627_-17+639delinsTGCAAAAGCCGCA
ENST00000688308.1:c.-17+156_-17+168delinsTGCAAAAGCCGCA (PTEN) ENSP00000508752.1:n.-17+156_-17+168delinsTGCAAAAGCCGCA
ENST00000445946.5:c.-794_-782delinsTGCGGCTTTTGCA (KLLN) MANE Select ENSP00000392204.2:n.-794_-782delinsTGCGGCTTTTGCA
ENST00000371953.7:c.-1201_-1189delinsTGCAAAAGCCGCA (PTEN) ENSP00000361021.3:n.-1201_-1189delinsTGCAAAAGCCGCA
ENST00000445946.3:c.-794_-782delinsTGCGGCTTTTGCA (KLLN) ENSP00000392204.2:n.-794_-782delinsTGCGGCTTTTGCA
NM_001126049.1:c.-794_-782delinsTGCGGCTTTTGCA (KLLN) NP_001119521.1:n.-794_-782delinsTGCGGCTTTTGCA
NM_001126049.2:c.-794_-782delinsTGCGGCTTTTGCA (KLLN) MANE Select NP_001119521.1:n.-794_-782delinsTGCGGCTTTTGCA
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