Canonical Allele Identifier: CA2054318155
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1880062982

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107217_91107224dup , CM000674.2:g.91107217_91107224dup GRCh38
NC_000012.11:g.91500994_91501001dup , CM000674.1:g.91500994_91501001dup GRCh37
NC_000012.10:g.90025125_90025132dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000266718.5:c.862+901_862+908dup MANE Select ENSP00000266718.4:n.862+901_862+908dup
ENST00000266718.4:c.862+901_862+908dup ENSP00000266718.4:n.862+901_862+908dup
ENST00000546642.1:n.612+901_612+908dup
ENST00000548071.1:n.255+901_255+908dup
NM_002345.3:c.862+901_862+908dup NP_002336.1:n.862+901_862+908dup
NM_002345.4:c.862+901_862+908dup MANE Select NP_002336.1:n.862+901_862+908dup