Canonical Allele Identifier: CA950429010
Gene: LUM HGNC NCBI

Linked Data

gnomAD v3: 12-91107184-A-AGAAG
gnomAD v4: 12-91107184-A-AGAAG
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107187_91107188insGGAA , CM000674.2:g.91107187_91107188insGGAA GRCh38
NC_000012.11:g.91500964_91500965insGGAA , CM000674.1:g.91500964_91500965insGGAA GRCh37
NC_000012.10:g.90025095_90025096insGGAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+933_862+934insCTTC MANE Select ENSP00000266718.4:n.862+933_862+934insCTTC
ENST00000266718.4:c.862+933_862+934insCTTC ENSP00000266718.4:n.862+933_862+934insCTTC
ENST00000546642.1:n.612+933_612+934insCTTC
ENST00000548071.1:n.255+933_255+934insCTTC
NM_002345.3:c.862+933_862+934insCTTC NP_002336.1:n.862+933_862+934insCTTC
NM_002345.4:c.862+933_862+934insCTTC MANE Select NP_002336.1:n.862+933_862+934insCTTC
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Search 100 bp 3'