Canonical Allele Identifier: CA2054318068
Gene: LUM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107150_91107159delinsAAAAAGAAAG , CM000674.2:g.91107150_91107159delinsAAAAAGAAAG GRCh38
NC_000012.11:g.91500927_91500936delinsAAAAAGAAAG , CM000674.1:g.91500927_91500936delinsAAAAAGAAAG GRCh37
NC_000012.10:g.90025058_90025067delinsAAAAAGAAAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+959_862+968delinsCTTTCTTTTT MANE Select ENSP00000266718.4:n.862+959_862+968delinsCTTTCTTTTT
ENST00000266718.4:c.862+959_862+968delinsCTTTCTTTTT ENSP00000266718.4:n.862+959_862+968delinsCTTTCTTTTT
ENST00000546642.1:n.612+959_612+968delinsCTTTCTTTTT
ENST00000548071.1:n.255+959_255+968delinsCTTTCTTTTT
NM_002345.3:c.862+959_862+968delinsCTTTCTTTTT NP_002336.1:n.862+959_862+968delinsCTTTCTTTTT
NM_002345.4:c.862+959_862+968delinsCTTTCTTTTT MANE Select NP_002336.1:n.862+959_862+968delinsCTTTCTTTTT