Canonical Allele Identifier: CA2054318367

Gene: LUM

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91107265_91107267delinsAAG , CM000674.2:g.91107265_91107267delinsAAG	GRCh38
NC_000012.11:g.91501042_91501044delinsAAG , CM000674.1:g.91501042_91501044delinsAAG	GRCh37
NC_000012.10:g.90025173_90025175delinsAAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.5:c.862+851_862+853delinsCTT MANE Select	ENSP00000266718.4:n.862+851_862+853delinsCTT
ENST00000266718.4:c.862+851_862+853delinsCTT	ENSP00000266718.4:n.862+851_862+853delinsCTT
ENST00000546642.1:n.612+851_612+853delinsCTT
ENST00000548071.1:n.255+851_255+853delinsCTT
NM_002345.3:c.862+851_862+853delinsCTT	NP_002336.1:n.862+851_862+853delinsCTT
NM_002345.4:c.862+851_862+853delinsCTT MANE Select	NP_002336.1:n.862+851_862+853delinsCTT