Canonical Allele Identifier: CA2054318177
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1880064051
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107217_91107221del , CM000674.2:g.91107217_91107221del GRCh38
NC_000012.11:g.91500994_91500998del , CM000674.1:g.91500994_91500998del GRCh37
NC_000012.10:g.90025125_90025129del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000266718.5:c.862+898_862+902del MANE Select ENSP00000266718.4:n.862+898_862+902del
ENST00000266718.4:c.862+898_862+902del ENSP00000266718.4:n.862+898_862+902del
ENST00000546642.1:n.612+898_612+902del
ENST00000548071.1:n.255+898_255+902del
NM_002345.3:c.862+898_862+902del NP_002336.1:n.862+898_862+902del
NM_002345.4:c.862+898_862+902del MANE Select NP_002336.1:n.862+898_862+902del
Search 100 bp 5'
Search 100 bp 3'