Canonical Allele Identifier: CA606703600
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1225884693
gnomAD v2: 12-91500990-AAGAG-A
gnomAD v3: 12-91107213-AAGAG-A
gnomAD v4: 12-91107213-AAGAG-A
MyVariant Identifiers: chr12:g.91500991_91500994del (hg19) chr12:g.91107214_91107217del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107217_91107220del , CM000674.2:g.91107217_91107220del GRCh38
NC_000012.11:g.91500994_91500997del , CM000674.1:g.91500994_91500997del GRCh37
NC_000012.10:g.90025125_90025128del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+901_862+904del MANE Select ENSP00000266718.4:n.862+901_862+904del
ENST00000266718.4:c.862+901_862+904del ENSP00000266718.4:n.862+901_862+904del
ENST00000546642.1:n.612+901_612+904del
ENST00000548071.1:n.255+901_255+904del
NM_002345.3:c.862+901_862+904del NP_002336.1:n.862+901_862+904del
NM_002345.4:c.862+901_862+904del MANE Select NP_002336.1:n.862+901_862+904del
Search 100 bp 5'
Search 100 bp 3'