Canonical Allele Identifier: CA2054318064

Gene: LUM

Linked Data

• dbSNP Id: rs773547125

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91107150_91107154del , CM000674.2:g.91107150_91107154del	GRCh38
NC_000012.11:g.91500927_91500931del , CM000674.1:g.91500927_91500931del	GRCh37
NC_000012.10:g.90025058_90025062del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.5:c.862+970_862+974del MANE Select	ENSP00000266718.4:n.862+970_862+974del
ENST00000266718.4:c.862+970_862+974del	ENSP00000266718.4:n.862+970_862+974del
ENST00000546642.1:n.612+970_612+974del
ENST00000548071.1:n.255+970_255+974del
NM_002345.3:c.862+970_862+974del	NP_002336.1:n.862+970_862+974del
NM_002345.4:c.862+970_862+974del MANE Select	NP_002336.1:n.862+970_862+974del