Canonical Allele Identifier: CA950429343
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1880073569
gnomAD v3: 12-91107251-GAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAGAAAGAAA-G
gnomAD v4: 12-91107251-GAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAGAAAGAAA-G
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107252_91107296del , CM000674.2:g.91107252_91107296del GRCh38
NC_000012.11:g.91501029_91501073del , CM000674.1:g.91501029_91501073del GRCh37
NC_000012.10:g.90025160_90025204del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000266718.5:c.862+822_862+866del MANE Select ENSP00000266718.4:n.862+822_862+866del
ENST00000266718.4:c.862+822_862+866del ENSP00000266718.4:n.862+822_862+866del
ENST00000546642.1:n.612+822_612+866del
ENST00000548071.1:n.255+822_255+866del
NM_002345.3:c.862+822_862+866del NP_002336.1:n.862+822_862+866del
NM_002345.4:c.862+822_862+866del MANE Select NP_002336.1:n.862+822_862+866del
Search 100 bp 5'
Search 100 bp 3'