Canonical Allele Identifier: CA606703696
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1491269418
gnomAD v2: 12-91501051-A-AG
gnomAD v3: 12-91107274-A-AG
gnomAD v4: 12-91107274-A-AG
MyVariant Identifiers: chr12:g.91501051_91501052insG (hg19) chr12:g.91107274_91107275insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107275dup , CM000674.2:g.91107275dup GRCh38
NC_000012.11:g.91501052dup , CM000674.1:g.91501052dup GRCh37
NC_000012.10:g.90025183dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+843dup MANE Select ENSP00000266718.4:n.862+843dup
ENST00000266718.4:c.862+843dup ENSP00000266718.4:n.862+843dup
ENST00000546642.1:n.612+843dup
ENST00000548071.1:n.255+843dup
NM_002345.3:c.862+843dup NP_002336.1:n.862+843dup
NM_002345.4:c.862+843dup MANE Select NP_002336.1:n.862+843dup
Search 100 bp 5'
Search 100 bp 3'