Canonical Allele Identifier: CA2600912210
Gene: LUM HGNC NCBI

Linked Data

gnomAD v3: 12-91107225-A-AAG
gnomAD v4: 12-91107225-A-AAG
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107225_91107226insAG , CM000674.2:g.91107225_91107226insAG GRCh38
NC_000012.11:g.91501002_91501003insAG , CM000674.1:g.91501002_91501003insAG GRCh37
NC_000012.10:g.90025133_90025134insAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+892_862+893insCT MANE Select ENSP00000266718.4:n.862+892_862+893insCT
ENST00000266718.4:c.862+892_862+893insCT ENSP00000266718.4:n.862+892_862+893insCT
ENST00000546642.1:n.612+892_612+893insCT
ENST00000548071.1:n.255+892_255+893insCT
NM_002345.3:c.862+892_862+893insCT NP_002336.1:n.862+892_862+893insCT
NM_002345.4:c.862+892_862+893insCT MANE Select NP_002336.1:n.862+892_862+893insCT
Search 100 bp 5'
Search 100 bp 3'