Canonical Allele Identifier: CA950428987

Gene: LUM

Linked Data

• dbSNP Id: rs1880057391
• gnomAD v3: 12-91107179-AAG-A
• gnomAD v4: 12-91107179-AAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91107181_91107182del , CM000674.2:g.91107181_91107182del	GRCh38
NC_000012.11:g.91500958_91500959del , CM000674.1:g.91500958_91500959del	GRCh37
NC_000012.10:g.90025089_90025090del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.5:c.862+937_862+938del MANE Select	ENSP00000266718.4:n.862+937_862+938del
ENST00000266718.4:c.862+937_862+938del	ENSP00000266718.4:n.862+937_862+938del
ENST00000546642.1:n.612+937_612+938del
ENST00000548071.1:n.255+937_255+938del
NM_002345.3:c.862+937_862+938del	NP_002336.1:n.862+937_862+938del
NM_002345.4:c.862+937_862+938del MANE Select	NP_002336.1:n.862+937_862+938del