Canonical Allele Identifier: CA2548827696
Gene: LUM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107014_91107015insTA , CM000674.2:g.91107014_91107015insTA GRCh38
NC_000012.11:g.91500791_91500792insTA , CM000674.1:g.91500791_91500792insTA GRCh37
NC_000012.10:g.90024922_90024923insTA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+1104_862+1105insAT MANE Select ENSP00000266718.4:n.862+1104_862+1105insAT
ENST00000266718.4:c.862+1104_862+1105insAT ENSP00000266718.4:n.862+1104_862+1105insAT
ENST00000546642.1:n.612+1104_612+1105insAT
ENST00000548071.1:n.255+1104_255+1105insAT
NM_002345.3:c.862+1104_862+1105insAT NP_002336.1:n.862+1104_862+1105insAT
NM_002345.4:c.862+1104_862+1105insAT MANE Select NP_002336.1:n.862+1104_862+1105insAT