Canonical Allele Identifier: CA2054318755

Gene: LUM

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91107372_91107373delinsAG , CM000674.2:g.91107372_91107373delinsAG	GRCh38
NC_000012.11:g.91501149_91501150delinsAG , CM000674.1:g.91501149_91501150delinsAG	GRCh37
NC_000012.10:g.90025280_90025281delinsAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.5:c.862+745_862+746delinsCT MANE Select	ENSP00000266718.4:n.862+745_862+746delinsCT
ENST00000266718.4:c.862+745_862+746delinsCT	ENSP00000266718.4:n.862+745_862+746delinsCT
ENST00000546642.1:n.612+745_612+746delinsCT
ENST00000548071.1:n.255+745_255+746delinsCT
NM_002345.3:c.862+745_862+746delinsCT	NP_002336.1:n.862+745_862+746delinsCT
NM_002345.4:c.862+745_862+746delinsCT MANE Select	NP_002336.1:n.862+745_862+746delinsCT