Canonical Allele Identifier: CA950430027
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1880093149

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107306_91107308del , CM000674.2:g.91107306_91107308del GRCh38
NC_000012.11:g.91501083_91501085del , CM000674.1:g.91501083_91501085del GRCh37
NC_000012.10:g.90025214_90025216del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+810_862+812del MANE Select ENSP00000266718.4:n.862+810_862+812del
ENST00000266718.4:c.862+810_862+812del ENSP00000266718.4:n.862+810_862+812del
ENST00000546642.1:n.612+810_612+812del
ENST00000548071.1:n.255+810_255+812del
NM_002345.3:c.862+810_862+812del NP_002336.1:n.862+810_862+812del
NM_002345.4:c.862+810_862+812del MANE Select NP_002336.1:n.862+810_862+812del