Canonical Allele Identifier: CA2796947660
Gene: LUM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107261_91107304del , CM000674.2:g.91107261_91107304del GRCh38
NC_000012.11:g.91501038_91501081del , CM000674.1:g.91501038_91501081del GRCh37
NC_000012.10:g.90025169_90025212del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000266718.5:c.862+815_862+858del MANE Select ENSP00000266718.4:n.862+815_862+858del
ENST00000266718.4:c.862+815_862+858del ENSP00000266718.4:n.862+815_862+858del
ENST00000546642.1:n.612+815_612+858del
ENST00000548071.1:n.255+815_255+858del
NM_002345.3:c.862+815_862+858del NP_002336.1:n.862+815_862+858del
NM_002345.4:c.862+815_862+858del MANE Select NP_002336.1:n.862+815_862+858del