Canonical Allele Identifier: CA2054318100

Gene: LUM

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91107179_91107181delinsAAG , CM000674.2:g.91107179_91107181delinsAAG	GRCh38
NC_000012.11:g.91500956_91500958delinsAAG , CM000674.1:g.91500956_91500958delinsAAG	GRCh37
NC_000012.10:g.90025087_90025089delinsAAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.5:c.862+937_862+939delinsCTT MANE Select	ENSP00000266718.4:n.862+937_862+939delinsCTT
ENST00000266718.4:c.862+937_862+939delinsCTT	ENSP00000266718.4:n.862+937_862+939delinsCTT
ENST00000546642.1:n.612+937_612+939delinsCTT
ENST00000548071.1:n.255+937_255+939delinsCTT
NM_002345.3:c.862+937_862+939delinsCTT	NP_002336.1:n.862+937_862+939delinsCTT
NM_002345.4:c.862+937_862+939delinsCTT MANE Select	NP_002336.1:n.862+937_862+939delinsCTT