Canonical Allele Identifier: CA2054318216

Gene: LUM

Linked Data

• dbSNP Id: rs1880065996

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91107229_91107230insAGAAAG , CM000674.2:g.91107229_91107230insAGAAAG	GRCh38
NC_000012.11:g.91501006_91501007insAGAAAG , CM000674.1:g.91501006_91501007insAGAAAG	GRCh37
NC_000012.10:g.90025137_90025138insAGAAAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.5:c.862+888_862+889insCTTTCT MANE Select	ENSP00000266718.4:n.862+888_862+889insCTTTCT
ENST00000266718.4:c.862+888_862+889insCTTTCT	ENSP00000266718.4:n.862+888_862+889insCTTTCT
ENST00000546642.1:n.612+888_612+889insCTTTCT
ENST00000548071.1:n.255+888_255+889insCTTTCT
NM_002345.3:c.862+888_862+889insCTTTCT	NP_002336.1:n.862+888_862+889insCTTTCT
NM_002345.4:c.862+888_862+889insCTTTCT MANE Select	NP_002336.1:n.862+888_862+889insCTTTCT