Canonical Allele Identifier: CA950430189

Gene: LUM

Linked Data

• dbSNP Id: rs1880097783
• gnomAD v3: 12-91107321-GAAA-G
• gnomAD v4: 12-91107321-GAAA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91107322_91107324del , CM000674.2:g.91107322_91107324del	GRCh38
NC_000012.11:g.91501099_91501101del , CM000674.1:g.91501099_91501101del	GRCh37
NC_000012.10:g.90025230_90025232del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.5:c.862+794_862+796del MANE Select	ENSP00000266718.4:n.862+794_862+796del
ENST00000266718.4:c.862+794_862+796del	ENSP00000266718.4:n.862+794_862+796del
ENST00000546642.1:n.612+794_612+796del
ENST00000548071.1:n.255+794_255+796del
NM_002345.3:c.862+794_862+796del	NP_002336.1:n.862+794_862+796del
NM_002345.4:c.862+794_862+796del MANE Select	NP_002336.1:n.862+794_862+796del