Canonical Allele Identifier: CA2054318754

Gene: LUM

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91107372_91107379delinsAGAGAGAG , CM000674.2:g.91107372_91107379delinsAGAGAGAG	GRCh38
NC_000012.11:g.91501149_91501156delinsAGAGAGAG , CM000674.1:g.91501149_91501156delinsAGAGAGAG	GRCh37
NC_000012.10:g.90025280_90025287delinsAGAGAGAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.5:c.862+739_862+746delinsCTCTCTCT MANE Select	ENSP00000266718.4:n.862+739_862+746delinsCTCTCTCT
ENST00000266718.4:c.862+739_862+746delinsCTCTCTCT	ENSP00000266718.4:n.862+739_862+746delinsCTCTCTCT
ENST00000546642.1:n.612+739_612+746delinsCTCTCTCT
ENST00000548071.1:n.255+739_255+746delinsCTCTCTCT
NM_002345.3:c.862+739_862+746delinsCTCTCTCT	NP_002336.1:n.862+739_862+746delinsCTCTCTCT
NM_002345.4:c.862+739_862+746delinsCTCTCTCT MANE Select	NP_002336.1:n.862+739_862+746delinsCTCTCTCT