Canonical Allele Identifier: CA241230226
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs368635211
gnomAD v2: 12-91501001-A-AG
gnomAD v3: 12-91107224-A-AG
gnomAD v4: 12-91107224-A-AG
MyVariant Identifiers: chr12:g.91501001_91501002insG (hg19) chr12:g.91107224_91107225insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107224_91107225insG , CM000674.2:g.91107224_91107225insG GRCh38
NC_000012.11:g.91501001_91501002insG , CM000674.1:g.91501001_91501002insG GRCh37
NC_000012.10:g.90025132_90025133insG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000266718.5:c.862+893_862+894insC MANE Select ENSP00000266718.4:n.862+893_862+894insC
ENST00000266718.4:c.862+893_862+894insC ENSP00000266718.4:n.862+893_862+894insC
ENST00000546642.1:n.612+893_612+894insC
ENST00000548071.1:n.255+893_255+894insC
NM_002345.3:c.862+893_862+894insC NP_002336.1:n.862+893_862+894insC
NM_002345.4:c.862+893_862+894insC MANE Select NP_002336.1:n.862+893_862+894insC
Search 100 bp 5'
Search 100 bp 3'