Canonical Allele Identifier: CA2054318137
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs140231552

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107202dup , CM000674.2:g.91107202dup GRCh38
NC_000012.11:g.91500979dup , CM000674.1:g.91500979dup GRCh37
NC_000012.10:g.90025110dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+920dup MANE Select ENSP00000266718.4:n.862+920dup
ENST00000266718.4:c.862+920dup ENSP00000266718.4:n.862+920dup
ENST00000546642.1:n.612+920dup
ENST00000548071.1:n.255+920dup
NM_002345.3:c.862+920dup NP_002336.1:n.862+920dup
NM_002345.4:c.862+920dup MANE Select NP_002336.1:n.862+920dup