Canonical Allele Identifier: CA2610045363

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863052_87863059del , CM000672.2:g.87863052_87863059del GRCh38
NC_000010.10:g.89622809_89622816del , CM000672.1:g.89622809_89622816del GRCh37
NC_000010.9:g.89612789_89612796del NCBI36
NG_007466.2:g.4615_4622del , LRG_311:g.4615_4622del
NG_033079.1:g.5380_5387del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+410_-17+417del (PTEN) ENSP00000516674.1:n.-17+410_-17+417del
ENST00000688308.1:c.-78_-71del (PTEN) ENSP00000508752.1:n.-78_-71del
ENST00000445946.5:c.-571_-564del (KLLN) MANE Select ENSP00000392204.2:n.-571_-564del
ENST00000445946.3:c.-571_-564del (KLLN) ENSP00000392204.2:n.-571_-564del
NM_001126049.1:c.-571_-564del (KLLN) NP_001119521.1:n.-571_-564del
NM_001126049.2:c.-571_-564del (KLLN) MANE Select NP_001119521.1:n.-571_-564del