Canonical Allele Identifier: CA950429029

Gene: LUM

Linked Data

• dbSNP Id: rs1880058601
• gnomAD v3: 12-91107189-G-GAA
• gnomAD v4: 12-91107189-G-GAA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91107190_91107191dup , CM000674.2:g.91107190_91107191dup	GRCh38
NC_000012.11:g.91500967_91500968dup , CM000674.1:g.91500967_91500968dup	GRCh37
NC_000012.10:g.90025098_90025099dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.5:c.862+927_862+928dup MANE Select	ENSP00000266718.4:n.862+927_862+928dup
ENST00000266718.4:c.862+927_862+928dup	ENSP00000266718.4:n.862+927_862+928dup
ENST00000546642.1:n.612+927_612+928dup
ENST00000548071.1:n.255+927_255+928dup
NM_002345.3:c.862+927_862+928dup	NP_002336.1:n.862+927_862+928dup
NM_002345.4:c.862+927_862+928dup MANE Select	NP_002336.1:n.862+927_862+928dup