Canonical Allele Identifier: CA2600912208
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs2121046345
gnomAD v3: 12-91107221-A-AAGAG
gnomAD v4: 12-91107221-A-AAGAG
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107224_91107225insGAGA , CM000674.2:g.91107224_91107225insGAGA GRCh38
NC_000012.11:g.91501001_91501002insGAGA , CM000674.1:g.91501001_91501002insGAGA GRCh37
NC_000012.10:g.90025132_90025133insGAGA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+896_862+897insCTCT MANE Select ENSP00000266718.4:n.862+896_862+897insCTCT
ENST00000266718.4:c.862+896_862+897insCTCT ENSP00000266718.4:n.862+896_862+897insCTCT
ENST00000546642.1:n.612+896_612+897insCTCT
ENST00000548071.1:n.255+896_255+897insCTCT
NM_002345.3:c.862+896_862+897insCTCT NP_002336.1:n.862+896_862+897insCTCT
NM_002345.4:c.862+896_862+897insCTCT MANE Select NP_002336.1:n.862+896_862+897insCTCT
Search 100 bp 5'
Search 100 bp 3'