Canonical Allele Identifier: CA2054318067

Gene: LUM

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91107150_91107155delinsAAAAAG , CM000674.2:g.91107150_91107155delinsAAAAAG	GRCh38
NC_000012.11:g.91500927_91500932delinsAAAAAG , CM000674.1:g.91500927_91500932delinsAAAAAG	GRCh37
NC_000012.10:g.90025058_90025063delinsAAAAAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.5:c.862+963_862+968delinsCTTTTT MANE Select	ENSP00000266718.4:n.862+963_862+968delinsCTTTTT
ENST00000266718.4:c.862+963_862+968delinsCTTTTT	ENSP00000266718.4:n.862+963_862+968delinsCTTTTT
ENST00000546642.1:n.612+963_612+968delinsCTTTTT
ENST00000548071.1:n.255+963_255+968delinsCTTTTT
NM_002345.3:c.862+963_862+968delinsCTTTTT	NP_002336.1:n.862+963_862+968delinsCTTTTT
NM_002345.4:c.862+963_862+968delinsCTTTTT MANE Select	NP_002336.1:n.862+963_862+968delinsCTTTTT