Canonical Allele Identifier: CA2610045330

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863039_87863040del , CM000672.2:g.87863039_87863040del GRCh38
NC_000010.10:g.89622796_89622797del , CM000672.1:g.89622796_89622797del GRCh37
NC_000010.9:g.89612776_89612777del NCBI36
NG_007466.2:g.4602_4603del , LRG_311:g.4602_4603del
NG_033079.1:g.5400_5401del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+397_-17+398del (PTEN) ENSP00000516674.1:n.-17+397_-17+398del
ENST00000688308.1:c.-91_-90del (PTEN) ENSP00000508752.1:n.-91_-90del
ENST00000445946.5:c.-551_-550del (KLLN) MANE Select ENSP00000392204.2:n.-551_-550del
ENST00000445946.3:c.-551_-550del (KLLN) ENSP00000392204.2:n.-551_-550del
NM_001126049.1:c.-551_-550del (KLLN) NP_001119521.1:n.-551_-550del
NM_001126049.2:c.-551_-550del (KLLN) MANE Select NP_001119521.1:n.-551_-550del