Canonical Allele Identifier: CA606703585
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1456921076
gnomAD v2: 12-91500927-AAAAAG-A
gnomAD v3: 12-91107150-AAAAAG-A
gnomAD v4: 12-91107150-AAAAAG-A
MyVariant Identifiers: chr12:g.91500928_91500932del (hg19) chr12:g.91107151_91107155del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107154_91107158del , CM000674.2:g.91107154_91107158del GRCh38
NC_000012.11:g.91500931_91500935del , CM000674.1:g.91500931_91500935del GRCh37
NC_000012.10:g.90025062_90025066del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+963_862+967del MANE Select ENSP00000266718.4:n.862+963_862+967del
ENST00000266718.4:c.862+963_862+967del ENSP00000266718.4:n.862+963_862+967del
ENST00000546642.1:n.612+963_612+967del
ENST00000548071.1:n.255+963_255+967del
NM_002345.3:c.862+963_862+967del NP_002336.1:n.862+963_862+967del
NM_002345.4:c.862+963_862+967del MANE Select NP_002336.1:n.862+963_862+967del
Search 100 bp 5'
Search 100 bp 3'