Canonical Allele Identifier: CA653885770
Gene: PTEN HGNC NCBI
KLLN HGNC NCBI

Linked Data

COSMIC: COSN20868123
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863494_87863495insC , CM000672.2:g.87863494_87863495insC GRCh38
NC_000010.10:g.89623251_89623252insC , CM000672.1:g.89623251_89623252insC GRCh37
NC_000010.9:g.89613231_89613232insC NCBI36
NG_007466.2:g.5057_5058insC , LRG_311:g.5057_5058insC
NG_033079.1:g.4943_4944insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+852_-17+853insC (PTEN) ENSP00000516674.1:n.-17+852_-17+853insC
ENST00000688308.1:c.-17+381_-17+382insC (PTEN) ENSP00000508752.1:n.-17+381_-17+382insC
ENST00000693560.1:c.-456_-455insC (PTEN) ENSP00000509861.1:n.-456_-455insC
ENST00000445946.5:c.-1008_-1007insG (KLLN) MANE Select ENSP00000392204.2:n.-1008_-1007insG
ENST00000371953.7:c.-976_-975insC (PTEN) ENSP00000361021.3:n.-976_-975insC
ENST00000610634.1:c.-1078_-1077insC (PTEN) ENSP00000477517.1:n.-1078_-1077insC
NM_000314.5:c.-975_-974insC (PTEN) NP_000305.3:n.-975_-974insC
NM_000314.6:c.-975_-974insC (PTEN) NP_000305.3:n.-975_-974insC
NM_001304717.2:c.-456_-455insC (PTEN) NP_001291646.2:n.-456_-455insC
NM_001304718.1:c.-1680_-1679insC (PTEN) NP_001291647.1:n.-1680_-1679insC
NM_001126049.2:c.-1008_-1007insG (KLLN) MANE Select NP_001119521.1:n.-1008_-1007insG
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