Canonical Allele Identifier: CA2610045447

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863093del , CM000672.2:g.87863093del GRCh38
NC_000010.10:g.89622850del , CM000672.1:g.89622850del GRCh37
NC_000010.9:g.89612830del NCBI36
NG_007466.2:g.4656del , LRG_311:g.4656del
NG_033079.1:g.5346del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+451del (PTEN) ENSP00000516674.1:n.-17+451del
ENST00000688308.1:c.-37del (PTEN) ENSP00000508752.1:n.-37del
ENST00000445946.5:c.-605del (KLLN) MANE Select ENSP00000392204.2:n.-605del
ENST00000445946.3:c.-605del (KLLN) ENSP00000392204.2:n.-605del
NM_001126049.1:c.-605del (KLLN) NP_001119521.1:n.-605del
NM_001126049.2:c.-605del (KLLN) MANE Select NP_001119521.1:n.-605del