Canonical Allele Identifier: CA2054318663

Gene: LUM

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91107327_91107329delinsAAG , CM000674.2:g.91107327_91107329delinsAAG	GRCh38
NC_000012.11:g.91501104_91501106delinsAAG , CM000674.1:g.91501104_91501106delinsAAG	GRCh37
NC_000012.10:g.90025235_90025237delinsAAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.5:c.862+789_862+791delinsCTT MANE Select	ENSP00000266718.4:n.862+789_862+791delinsCTT
ENST00000266718.4:c.862+789_862+791delinsCTT	ENSP00000266718.4:n.862+789_862+791delinsCTT
ENST00000546642.1:n.612+789_612+791delinsCTT
ENST00000548071.1:n.255+789_255+791delinsCTT
NM_002345.3:c.862+789_862+791delinsCTT	NP_002336.1:n.862+789_862+791delinsCTT
NM_002345.4:c.862+789_862+791delinsCTT MANE Select	NP_002336.1:n.862+789_862+791delinsCTT