Canonical Allele Identifier: CA950428873
Gene: LUM HGNC NCBI

Linked Data

gnomAD v3: 12-91107143-CAAA-C
gnomAD v4: 12-91107143-CAAA-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107152_91107154del , CM000674.2:g.91107152_91107154del GRCh38
NC_000012.11:g.91500929_91500931del , CM000674.1:g.91500929_91500931del GRCh37
NC_000012.10:g.90025060_90025062del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+972_862+974del MANE Select ENSP00000266718.4:n.862+972_862+974del
ENST00000266718.4:c.862+972_862+974del ENSP00000266718.4:n.862+972_862+974del
ENST00000546642.1:n.612+972_612+974del
ENST00000548071.1:n.255+972_255+974del
NM_002345.3:c.862+972_862+974del NP_002336.1:n.862+972_862+974del
NM_002345.4:c.862+972_862+974del MANE Select NP_002336.1:n.862+972_862+974del
Search 100 bp 5'
Search 100 bp 3'