Canonical Allele Identifier: CA606703767
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1565758464
gnomAD v2: 12-91501076-A-AG
gnomAD v3: 12-91107299-A-AG
gnomAD v4: 12-91107299-A-AG
MyVariant Identifiers: chr12:g.91501076_91501077insG (hg19) chr12:g.91107299_91107300insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107299_91107300insG , CM000674.2:g.91107299_91107300insG GRCh38
NC_000012.11:g.91501076_91501077insG , CM000674.1:g.91501076_91501077insG GRCh37
NC_000012.10:g.90025207_90025208insG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+818_862+819insC MANE Select ENSP00000266718.4:n.862+818_862+819insC
ENST00000266718.4:c.862+818_862+819insC ENSP00000266718.4:n.862+818_862+819insC
ENST00000546642.1:n.612+818_612+819insC
ENST00000548071.1:n.255+818_255+819insC
NM_002345.3:c.862+818_862+819insC NP_002336.1:n.862+818_862+819insC
NM_002345.4:c.862+818_862+819insC MANE Select NP_002336.1:n.862+818_862+819insC
Search 100 bp 5'
Search 100 bp 3'