Canonical Allele Identifier: CA950430230
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1880099825
gnomAD v3: 12-91107330-AAAGAAAGAAAGAAAGG-A
gnomAD v4: 12-91107330-AAAGAAAGAAAGAAAGG-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107331_91107346del , CM000674.2:g.91107331_91107346del GRCh38
NC_000012.11:g.91501108_91501123del , CM000674.1:g.91501108_91501123del GRCh37
NC_000012.10:g.90025239_90025254del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000266718.5:c.862+772_862+787del MANE Select ENSP00000266718.4:n.862+772_862+787del
ENST00000266718.4:c.862+772_862+787del ENSP00000266718.4:n.862+772_862+787del
ENST00000546642.1:n.612+772_612+787del
ENST00000548071.1:n.255+772_255+787del
NM_002345.3:c.862+772_862+787del NP_002336.1:n.862+772_862+787del
NM_002345.4:c.862+772_862+787del MANE Select NP_002336.1:n.862+772_862+787del
Search 100 bp 5'
Search 100 bp 3'