Canonical Allele Identifier: CA2600912232
Gene: LUM HGNC NCBI

Linked Data

gnomAD v3: 12-91107275-GAAAGAAAGAAAGAGAAA-G
gnomAD v4: 12-91107275-GAAAGAAAGAAAGAGAAA-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107276_91107292del , CM000674.2:g.91107276_91107292del GRCh38
NC_000012.11:g.91501053_91501069del , CM000674.1:g.91501053_91501069del GRCh37
NC_000012.10:g.90025184_90025200del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+826_862+842del MANE Select ENSP00000266718.4:n.862+826_862+842del
ENST00000266718.4:c.862+826_862+842del ENSP00000266718.4:n.862+826_862+842del
ENST00000546642.1:n.612+826_612+842del
ENST00000548071.1:n.255+826_255+842del
NM_002345.3:c.862+826_862+842del NP_002336.1:n.862+826_862+842del
NM_002345.4:c.862+826_862+842del MANE Select NP_002336.1:n.862+826_862+842del
Search 100 bp 5'
Search 100 bp 3'