Canonical Allele Identifier: CA950428783

Gene: LUM

Linked Data

• gnomAD v3: 12-91107050-G-GC
• gnomAD v4: 12-91107050-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91107050_91107051insC , CM000674.2:g.91107050_91107051insC	GRCh38
NC_000012.11:g.91500827_91500828insC , CM000674.1:g.91500827_91500828insC	GRCh37
NC_000012.10:g.90024958_90024959insC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.5:c.862+1067_862+1068insG MANE Select	ENSP00000266718.4:n.862+1067_862+1068insG
ENST00000266718.4:c.862+1067_862+1068insG	ENSP00000266718.4:n.862+1067_862+1068insG
ENST00000546642.1:n.612+1067_612+1068insG
ENST00000548071.1:n.255+1067_255+1068insG
NM_002345.3:c.862+1067_862+1068insG	NP_002336.1:n.862+1067_862+1068insG
NM_002345.4:c.862+1067_862+1068insG MANE Select	NP_002336.1:n.862+1067_862+1068insG