Canonical Allele Identifier: CA2054318454

Gene: LUM

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91107281_91107287delinsAAGAAAG , CM000674.2:g.91107281_91107287delinsAAGAAAG	GRCh38
NC_000012.11:g.91501058_91501064delinsAAGAAAG , CM000674.1:g.91501058_91501064delinsAAGAAAG	GRCh37
NC_000012.10:g.90025189_90025195delinsAAGAAAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.5:c.862+831_862+837delinsCTTTCTT MANE Select	ENSP00000266718.4:n.862+831_862+837delinsCTTTCTT
ENST00000266718.4:c.862+831_862+837delinsCTTTCTT	ENSP00000266718.4:n.862+831_862+837delinsCTTTCTT
ENST00000546642.1:n.612+831_612+837delinsCTTTCTT
ENST00000548071.1:n.255+831_255+837delinsCTTTCTT
NM_002345.3:c.862+831_862+837delinsCTTTCTT	NP_002336.1:n.862+831_862+837delinsCTTTCTT
NM_002345.4:c.862+831_862+837delinsCTTTCTT MANE Select	NP_002336.1:n.862+831_862+837delinsCTTTCTT