Canonical Allele Identifier: CA2796947640

Gene: LUM

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91107039_91107040insTCGCACTTCT , CM000674.2:g.91107039_91107040insTCGCACTTCT	GRCh38
NC_000012.11:g.91500816_91500817insTCGCACTTCT , CM000674.1:g.91500816_91500817insTCGCACTTCT	GRCh37
NC_000012.10:g.90024947_90024948insTCGCACTTCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.5:c.862+1078_862+1079insAGAAGTGCGA MANE Select	ENSP00000266718.4:n.862+1078_862+1079insAGAAGTGCGA
ENST00000266718.4:c.862+1078_862+1079insAGAAGTGCGA	ENSP00000266718.4:n.862+1078_862+1079insAGAAGTGCGA
ENST00000546642.1:n.612+1078_612+1079insAGAAGTGCGA
ENST00000548071.1:n.255+1078_255+1079insAGAAGTGCGA
NM_002345.3:c.862+1078_862+1079insAGAAGTGCGA	NP_002336.1:n.862+1078_862+1079insAGAAGTGCGA
NM_002345.4:c.862+1078_862+1079insAGAAGTGCGA MANE Select	NP_002336.1:n.862+1078_862+1079insAGAAGTGCGA