Canonical Allele Identifier: CA950428926
Gene: LUM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107159_91107160del , CM000674.2:g.91107159_91107160del GRCh38
NC_000012.11:g.91500936_91500937del , CM000674.1:g.91500936_91500937del GRCh37
NC_000012.10:g.90025067_90025068del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+959_862+960del MANE Select ENSP00000266718.4:n.862+959_862+960del
ENST00000266718.4:c.862+959_862+960del ENSP00000266718.4:n.862+959_862+960del
ENST00000546642.1:n.612+959_612+960del
ENST00000548071.1:n.255+959_255+960del
NM_002345.3:c.862+959_862+960del NP_002336.1:n.862+959_862+960del
NM_002345.4:c.862+959_862+960del MANE Select NP_002336.1:n.862+959_862+960del