Canonical Allele Identifier: CA2054318108

Gene: LUM

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91107183_91107185delinsAAG , CM000674.2:g.91107183_91107185delinsAAG	GRCh38
NC_000012.11:g.91500960_91500962delinsAAG , CM000674.1:g.91500960_91500962delinsAAG	GRCh37
NC_000012.10:g.90025091_90025093delinsAAG	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000266718.5:c.862+933_862+935delinsCTT MANE Select	ENSP00000266718.4:n.862+933_862+935delinsCTT
ENST00000266718.4:c.862+933_862+935delinsCTT	ENSP00000266718.4:n.862+933_862+935delinsCTT
ENST00000546642.1:n.612+933_612+935delinsCTT
ENST00000548071.1:n.255+933_255+935delinsCTT
NM_002345.3:c.862+933_862+935delinsCTT	NP_002336.1:n.862+933_862+935delinsCTT
NM_002345.4:c.862+933_862+935delinsCTT MANE Select	NP_002336.1:n.862+933_862+935delinsCTT