Canonical Allele Identifier: CA2788894864
Gene: PTEN HGNC NCBI
KLLN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863529_87863531del , CM000672.2:g.87863529_87863531del GRCh38
NC_000010.10:g.89623286_89623288del , CM000672.1:g.89623286_89623288del GRCh37
NC_000010.9:g.89613266_89613268del NCBI36
NG_007466.2:g.5092_5094del , LRG_311:g.5092_5094del
NG_033079.1:g.4914_4916del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+887_-17+889del (PTEN) ENSP00000516674.1:n.-17+887_-17+889del
ENST00000688308.1:c.-17+416_-17+418del (PTEN) ENSP00000508752.1:n.-17+416_-17+418del
ENST00000693560.1:c.-421_-419del (PTEN) ENSP00000509861.1:n.-421_-419del
ENST00000445946.5:c.-1037_-1035del (KLLN) MANE Select ENSP00000392204.2:n.-1037_-1035del
ENST00000371953.7:c.-941_-939del (PTEN) ENSP00000361021.3:n.-941_-939del
ENST00000610634.1:c.-1043_-1041del (PTEN) ENSP00000477517.1:n.-1043_-1041del
NM_000314.5:c.-940_-938del (PTEN) NP_000305.3:n.-940_-938del
NM_000314.6:c.-940_-938del (PTEN) NP_000305.3:n.-940_-938del
NM_001304717.2:c.-421_-419del (PTEN) NP_001291646.2:n.-421_-419del
NM_001304718.1:c.-1645_-1643del (PTEN) NP_001291647.1:n.-1645_-1643del
NM_001126049.2:c.-1037_-1035del (KLLN) MANE Select NP_001119521.1:n.-1037_-1035del
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