Canonical Allele Identifier: CA606703573
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs906938900
gnomAD v2: 12-91500805-CTGG-C
gnomAD v3: 12-91107028-CTGG-C
gnomAD v4: 12-91107028-CTGG-C
MyVariant Identifiers: chr12:g.91500806_91500808del (hg19) chr12:g.91107029_91107031del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107041_91107043del , CM000674.2:g.91107041_91107043del GRCh38
NC_000012.11:g.91500818_91500820del , CM000674.1:g.91500818_91500820del GRCh37
NC_000012.10:g.90024949_90024951del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+1087_862+1089del MANE Select ENSP00000266718.4:n.862+1087_862+1089del
ENST00000266718.4:c.862+1087_862+1089del ENSP00000266718.4:n.862+1087_862+1089del
ENST00000546642.1:n.612+1087_612+1089del
ENST00000548071.1:n.255+1087_255+1089del
NM_002345.3:c.862+1087_862+1089del NP_002336.1:n.862+1087_862+1089del
NM_002345.4:c.862+1087_862+1089del MANE Select NP_002336.1:n.862+1087_862+1089del
Search 100 bp 5'
Search 100 bp 3'