Canonical Allele Identifier: CA2610045347

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863045_87863047del , CM000672.2:g.87863045_87863047del GRCh38
NC_000010.10:g.89622802_89622804del , CM000672.1:g.89622802_89622804del GRCh37
NC_000010.9:g.89612782_89612784del NCBI36
NG_007466.2:g.4608_4610del , LRG_311:g.4608_4610del
NG_033079.1:g.5391_5393del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+403_-17+405del (PTEN) ENSP00000516674.1:n.-17+403_-17+405del
ENST00000688308.1:c.-85_-83del (PTEN) ENSP00000508752.1:n.-85_-83del
ENST00000445946.5:c.-560_-558del (KLLN) MANE Select ENSP00000392204.2:n.-560_-558del
ENST00000445946.3:c.-560_-558del (KLLN) ENSP00000392204.2:n.-560_-558del
NM_001126049.1:c.-560_-558del (KLLN) NP_001119521.1:n.-560_-558del
NM_001126049.2:c.-560_-558del (KLLN) MANE Select NP_001119521.1:n.-560_-558del