Canonical Allele Identifier: CA1926142656
Gene: PTEN HGNC NCBI
KLLN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863009_87863025delinsAGGGGTAGAGGCAAGGG , CM000672.2:g.87863009_87863025delinsAGGGGTAGAGGCAAGGG GRCh38
NC_000010.10:g.89622766_89622782delinsAGGGGTAGAGGCAAGGG , CM000672.1:g.89622766_89622782delinsAGGGGTAGAGGCAAGGG GRCh37
NC_000010.9:g.89612746_89612762delinsAGGGGTAGAGGCAAGGG NCBI36
NG_007466.2:g.4572_4588delinsAGGGGTAGAGGCAAGGG , LRG_311:g.4572_4588delinsAGGGGTAGAGGCAAGGG
NG_033079.1:g.5413_5429delinsCCCTTGCCTCTACCCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+367_-17+383delinsAGGGGTAGAGGCAAGGG (PTEN) ENSP00000516674.1:n.-17+367_-17+383delinsAGGGGTAGAGGCAAGGG
ENST00000688308.1:c.-121_-105delinsAGGGGTAGAGGCAAGGG (PTEN) ENSP00000508752.1:n.-121_-105delinsAGGGGTAGAGGCAAGGG
ENST00000445946.5:c.-538_-522delinsCCCTTGCCTCTACCCCT (KLLN) MANE Select ENSP00000392204.2:n.-538_-522delinsCCCTTGCCTCTACCCCT
ENST00000445946.3:c.-538_-522delinsCCCTTGCCTCTACCCCT (KLLN) ENSP00000392204.2:n.-538_-522delinsCCCTTGCCTCTACCCCT
NM_001126049.1:c.-538_-522delinsCCCTTGCCTCTACCCCT (KLLN) NP_001119521.1:n.-538_-522delinsCCCTTGCCTCTACCCCT
NM_001126049.2:c.-538_-522delinsCCCTTGCCTCTACCCCT (KLLN) MANE Select NP_001119521.1:n.-538_-522delinsCCCTTGCCTCTACCCCT
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