Canonical Allele Identifier: CA950429022

Gene: LUM

Linked Data

• dbSNP Id: rs1880058226
• gnomAD v3: 12-91107187-A-T
• gnomAD v4: 12-91107187-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91107187A>T , CM000674.2:g.91107187A>T	GRCh38
NC_000012.11:g.91500964A>T , CM000674.1:g.91500964A>T	GRCh37
NC_000012.10:g.90025095A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.5:c.862+931T>A MANE Select	ENSP00000266718.4:n.862+931T>A
ENST00000266718.4:c.862+931T>A	ENSP00000266718.4:n.862+931T>A
ENST00000546642.1:n.612+931T>A
ENST00000548071.1:n.255+931T>A
NM_002345.3:c.862+931T>A	NP_002336.1:n.862+931T>A
NM_002345.4:c.862+931T>A MANE Select	NP_002336.1:n.862+931T>A