Canonical Allele Identifier: CA1926142989
Gene: PTEN HGNC NCBI
KLLN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863436_87863441delinsGCCCTC , CM000672.2:g.87863436_87863441delinsGCCCTC GRCh38
NC_000010.10:g.89623193_89623198delinsGCCCTC , CM000672.1:g.89623193_89623198delinsGCCCTC GRCh37
NC_000010.9:g.89613173_89613178delinsGCCCTC NCBI36
NG_007466.2:g.4999_5004delinsGCCCTC , LRG_311:g.4999_5004delinsGCCCTC
NG_033079.1:g.4997_5002delinsGAGGGC

Transcript Alleles

HGVS Amino-acid change
ENST00000706954.1:c.-17+794_-17+799delinsGCCCTC (PTEN) ENSP00000516674.1:n.-17+794_-17+799delinsGCCCTC
ENST00000688308.1:c.-17+323_-17+328delinsGCCCTC (PTEN) ENSP00000508752.1:n.-17+323_-17+328delinsGCCCTC
ENST00000445946.5:c.-954_-949delinsGAGGGC (KLLN) MANE Select ENSP00000392204.2:n.-954_-949delinsGAGGGC
ENST00000371953.7:c.-1034_-1029delinsGCCCTC (PTEN) ENSP00000361021.3:n.-1034_-1029delinsGCCCTC
NM_001126049.2:c.-954_-949delinsGAGGGC (KLLN) MANE Select NP_001119521.1:n.-954_-949delinsGAGGGC
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