Canonical Allele Identifier: CA2796947644
Gene: LUM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107201_91107202insGAA , CM000674.2:g.91107201_91107202insGAA GRCh38
NC_000012.11:g.91500978_91500979insGAA , CM000674.1:g.91500978_91500979insGAA GRCh37
NC_000012.10:g.90025109_90025110insGAA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000266718.5:c.862+918_862+919insCTT MANE Select ENSP00000266718.4:n.862+918_862+919insCTT
ENST00000266718.4:c.862+918_862+919insCTT ENSP00000266718.4:n.862+918_862+919insCTT
ENST00000546642.1:n.612+918_612+919insCTT
ENST00000548071.1:n.255+918_255+919insCTT
NM_002345.3:c.862+918_862+919insCTT NP_002336.1:n.862+918_862+919insCTT
NM_002345.4:c.862+918_862+919insCTT MANE Select NP_002336.1:n.862+918_862+919insCTT