Canonical Allele Identifier: CA2519350152
Gene: LUM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107384_91107385del , CM000674.2:g.91107384_91107385del GRCh38
NC_000012.11:g.91501161_91501162del , CM000674.1:g.91501161_91501162del GRCh37
NC_000012.10:g.90025292_90025293del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+734_862+735del MANE Select ENSP00000266718.4:n.862+734_862+735del
ENST00000266718.4:c.862+734_862+735del ENSP00000266718.4:n.862+734_862+735del
ENST00000546642.1:n.612+734_612+735del
ENST00000548071.1:n.255+734_255+735del
NM_002345.3:c.862+734_862+735del NP_002336.1:n.862+734_862+735del
NM_002345.4:c.862+734_862+735del MANE Select NP_002336.1:n.862+734_862+735del