Canonical Allele Identifier: CA606703617
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1555188589
gnomAD v2: 12-91501015-GGAAA-G
gnomAD v3: 12-91107238-GGAAA-G
gnomAD v4: 12-91107238-GGAAA-G
MyVariant Identifiers: chr12:g.91501016_91501019del (hg19) chr12:g.91107239_91107242del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107285_91107288del , CM000674.2:g.91107285_91107288del GRCh38
NC_000012.11:g.91501062_91501065del , CM000674.1:g.91501062_91501065del GRCh37
NC_000012.10:g.90025193_90025196del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+876_862+879del MANE Select ENSP00000266718.4:n.862+876_862+879del
ENST00000266718.4:c.862+876_862+879del ENSP00000266718.4:n.862+876_862+879del
ENST00000546642.1:n.612+876_612+879del
ENST00000548071.1:n.255+876_255+879del
NM_002345.3:c.862+876_862+879del NP_002336.1:n.862+876_862+879del
NM_002345.4:c.862+876_862+879del MANE Select NP_002336.1:n.862+876_862+879del
Search 100 bp 5'
Search 100 bp 3'