Canonical Allele Identifier: CA2054318131
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1880059119
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107192_91107197del , CM000674.2:g.91107192_91107197del GRCh38
NC_000012.11:g.91500969_91500974del , CM000674.1:g.91500969_91500974del GRCh37
NC_000012.10:g.90025100_90025105del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+921_862+926del MANE Select ENSP00000266718.4:n.862+921_862+926del
ENST00000266718.4:c.862+921_862+926del ENSP00000266718.4:n.862+921_862+926del
ENST00000546642.1:n.612+921_612+926del
ENST00000548071.1:n.255+921_255+926del
NM_002345.3:c.862+921_862+926del NP_002336.1:n.862+921_862+926del
NM_002345.4:c.862+921_862+926del MANE Select NP_002336.1:n.862+921_862+926del
Search 100 bp 5'
Search 100 bp 3'