Canonical Allele Identifier: CA2054318522

Gene: LUM

Linked Data

• dbSNP Id: rs1565758440

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91107296_91107300dup , CM000674.2:g.91107296_91107300dup	GRCh38
NC_000012.11:g.91501073_91501077dup , CM000674.1:g.91501073_91501077dup	GRCh37
NC_000012.10:g.90025204_90025208dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.5:c.862+820_862+824dup MANE Select	ENSP00000266718.4:n.862+820_862+824dup
ENST00000266718.4:c.862+820_862+824dup	ENSP00000266718.4:n.862+820_862+824dup
ENST00000546642.1:n.612+820_612+824dup
ENST00000548071.1:n.255+820_255+824dup
NM_002345.3:c.862+820_862+824dup	NP_002336.1:n.862+820_862+824dup
NM_002345.4:c.862+820_862+824dup MANE Select	NP_002336.1:n.862+820_862+824dup