Canonical Allele Identifier: CA481083468
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1555188581
gnomAD v2: 12-91501000-G-GA
gnomAD v3: 12-91107223-G-GA
gnomAD v4: 12-91107223-G-GA
MyVariant Identifiers: chr12:g.91501001_91501002insA (hg19) chr12:g.91501000_91501001insA (hg19) chr12:g.91107224_91107225insA (hg38) chr12:g.91107223_91107224insA (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+894dup MANE Select ENSP00000266718.4:n.862+894dup
ENST00000266718.4:c.862+894dup ENSP00000266718.4:n.862+894dup
ENST00000546642.1:n.612+894dup
ENST00000548071.1:n.255+894dup
NM_002345.3:c.862+894dup NP_002336.1:n.862+894dup
NM_002345.4:c.862+894dup MANE Select NP_002336.1:n.862+894dup
Search 100 bp 5'
Search 100 bp 3'