Canonical Allele Identifier: CA950429498

Gene: LUM

Linked Data

• dbSNP Id: rs1880080089
• gnomAD v3: 12-91107269-A-AAAG
• gnomAD v4: 12-91107269-A-AAAG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91107270_91107271insAGA , CM000674.2:g.91107270_91107271insAGA	GRCh38
NC_000012.11:g.91501047_91501048insAGA , CM000674.1:g.91501047_91501048insAGA	GRCh37
NC_000012.10:g.90025178_90025179insAGA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.5:c.862+848_862+849insCTT MANE Select	ENSP00000266718.4:n.862+848_862+849insCTT
ENST00000266718.4:c.862+848_862+849insCTT	ENSP00000266718.4:n.862+848_862+849insCTT
ENST00000546642.1:n.612+848_612+849insCTT
ENST00000548071.1:n.255+848_255+849insCTT
NM_002345.3:c.862+848_862+849insCTT	NP_002336.1:n.862+848_862+849insCTT
NM_002345.4:c.862+848_862+849insCTT MANE Select	NP_002336.1:n.862+848_862+849insCTT