Canonical Allele Identifier: CA950429355

Gene: LUM

Linked Data

• dbSNP Id: rs1880073738
• gnomAD v3: 12-91107253-A-AG
• gnomAD v4: 12-91107253-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91107253_91107254insG , CM000674.2:g.91107253_91107254insG	GRCh38
NC_000012.11:g.91501030_91501031insG , CM000674.1:g.91501030_91501031insG	GRCh37
NC_000012.10:g.90025161_90025162insG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.5:c.862+864_862+865insC MANE Select	ENSP00000266718.4:n.862+864_862+865insC
ENST00000266718.4:c.862+864_862+865insC	ENSP00000266718.4:n.862+864_862+865insC
ENST00000546642.1:n.612+864_612+865insC
ENST00000548071.1:n.255+864_255+865insC
NM_002345.3:c.862+864_862+865insC	NP_002336.1:n.862+864_862+865insC
NM_002345.4:c.862+864_862+865insC MANE Select	NP_002336.1:n.862+864_862+865insC