Canonical Allele Identifier: CA2546499774
Gene: LUM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107161_91107162del , CM000674.2:g.91107161_91107162del GRCh38
NC_000012.11:g.91500938_91500939del , CM000674.1:g.91500938_91500939del GRCh37
NC_000012.10:g.90025069_90025070del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+957_862+958del MANE Select ENSP00000266718.4:n.862+957_862+958del
ENST00000266718.4:c.862+957_862+958del ENSP00000266718.4:n.862+957_862+958del
ENST00000546642.1:n.612+957_612+958del
ENST00000548071.1:n.255+957_255+958del
NM_002345.3:c.862+957_862+958del NP_002336.1:n.862+957_862+958del
NM_002345.4:c.862+957_862+958del MANE Select NP_002336.1:n.862+957_862+958del