Canonical Allele Identifier: CA2054318489

Gene: LUM

Linked Data

• dbSNP Id: rs1880087626

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91107287_91107288insGAA , CM000674.2:g.91107287_91107288insGAA	GRCh38
NC_000012.11:g.91501064_91501065insGAA , CM000674.1:g.91501064_91501065insGAA	GRCh37
NC_000012.10:g.90025195_90025196insGAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.5:c.862+830_862+831insTTC MANE Select	ENSP00000266718.4:n.862+830_862+831insTTC
ENST00000266718.4:c.862+830_862+831insTTC	ENSP00000266718.4:n.862+830_862+831insTTC
ENST00000546642.1:n.612+830_612+831insTTC
ENST00000548071.1:n.255+830_255+831insTTC
NM_002345.3:c.862+830_862+831insTTC	NP_002336.1:n.862+830_862+831insTTC
NM_002345.4:c.862+830_862+831insTTC MANE Select	NP_002336.1:n.862+830_862+831insTTC