Canonical Allele Identifier: CA2610045309

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863029del , CM000672.2:g.87863029del GRCh38
NC_000010.10:g.89622786del , CM000672.1:g.89622786del GRCh37
NC_000010.9:g.89612766del NCBI36
NG_007466.2:g.4592del , LRG_311:g.4592del
NG_033079.1:g.5409del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+387del (PTEN) ENSP00000516674.1:n.-17+387del
ENST00000688308.1:c.-101del (PTEN) ENSP00000508752.1:n.-101del
ENST00000445946.5:c.-542del (KLLN) MANE Select ENSP00000392204.2:n.-542del
ENST00000445946.3:c.-542del (KLLN) ENSP00000392204.2:n.-542del
NM_001126049.1:c.-542del (KLLN) NP_001119521.1:n.-542del
NM_001126049.2:c.-542del (KLLN) MANE Select NP_001119521.1:n.-542del