Canonical Allele Identifier: CA606703587
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1376106129
gnomAD v2: 12-91500928-A-AG
gnomAD v3: 12-91107151-A-AG
gnomAD v4: 12-91107151-A-AG
MyVariant Identifiers: chr12:g.91500928_91500929insG (hg19) chr12:g.91500929_91500932delinsGAAAG (hg19) chr12:g.91107151_91107152insG (hg38) chr12:g.91107152_91107155delinsGAAAG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107151_91107152insG , CM000674.2:g.91107151_91107152insG GRCh38
NC_000012.11:g.91500928_91500929insG , CM000674.1:g.91500928_91500929insG GRCh37
NC_000012.10:g.90025059_90025060insG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+966_862+967insC MANE Select ENSP00000266718.4:n.862+966_862+967insC
ENST00000266718.4:c.862+966_862+967insC ENSP00000266718.4:n.862+966_862+967insC
ENST00000546642.1:n.612+966_612+967insC
ENST00000548071.1:n.255+966_255+967insC
NM_002345.3:c.862+966_862+967insC NP_002336.1:n.862+966_862+967insC
NM_002345.4:c.862+966_862+967insC MANE Select NP_002336.1:n.862+966_862+967insC
Search 100 bp 5'
Search 100 bp 3'