Canonical Allele Identifier: CA2796947641
Gene: LUM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107041_91107042insAATCCCAGCTACTCAGGA , CM000674.2:g.91107041_91107042insAATCCCAGCTACTCAGGA GRCh38
NC_000012.11:g.91500818_91500819insAATCCCAGCTACTCAGGA , CM000674.1:g.91500818_91500819insAATCCCAGCTACTCAGGA GRCh37
NC_000012.10:g.90024949_90024950insAATCCCAGCTACTCAGGA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+1076_862+1077insTCCTGAGTAGCTGGGATT MANE Select ENSP00000266718.4:n.862+1076_862+1077insTCCTGAGTAGCTGGGATT
ENST00000266718.4:c.862+1076_862+1077insTCCTGAGTAGCTGGGATT ENSP00000266718.4:n.862+1076_862+1077insTCCTGAGTAGCTGGGATT
ENST00000546642.1:n.612+1076_612+1077insTCCTGAGTAGCTGGGATT
ENST00000548071.1:n.255+1076_255+1077insTCCTGAGTAGCTGGGATT
NM_002345.3:c.862+1076_862+1077insTCCTGAGTAGCTGGGATT NP_002336.1:n.862+1076_862+1077insTCCTGAGTAGCTGGGATT
NM_002345.4:c.862+1076_862+1077insTCCTGAGTAGCTGGGATT MANE Select NP_002336.1:n.862+1076_862+1077insTCCTGAGTAGCTGGGATT