Canonical Allele Identifier: CA950429203
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1880069892
gnomAD v3: 12-91107238-GGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGA-G
gnomAD v4: 12-91107238-GGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGA-G
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107289_91107338del , CM000674.2:g.91107289_91107338del GRCh38
NC_000012.11:g.91501066_91501115del , CM000674.1:g.91501066_91501115del GRCh37
NC_000012.10:g.90025197_90025246del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000266718.5:c.862+830_862+879del MANE Select ENSP00000266718.4:n.862+830_862+879del
ENST00000266718.4:c.862+830_862+879del ENSP00000266718.4:n.862+830_862+879del
ENST00000546642.1:n.612+830_612+879del
ENST00000548071.1:n.255+830_255+879del
NM_002345.3:c.862+830_862+879del NP_002336.1:n.862+830_862+879del
NM_002345.4:c.862+830_862+879del MANE Select NP_002336.1:n.862+830_862+879del
Search 100 bp 5'
Search 100 bp 3'