Canonical Allele Identifier: CA2054318683
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1849278195

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107333_91107338dup , CM000674.2:g.91107333_91107338dup GRCh38
NC_000012.11:g.91501110_91501115dup , CM000674.1:g.91501110_91501115dup GRCh37
NC_000012.10:g.90025241_90025246dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+781_862+786dup MANE Select ENSP00000266718.4:n.862+781_862+786dup
ENST00000266718.4:c.862+781_862+786dup ENSP00000266718.4:n.862+781_862+786dup
ENST00000546642.1:n.612+781_612+786dup
ENST00000548071.1:n.255+781_255+786dup
NM_002345.3:c.862+781_862+786dup NP_002336.1:n.862+781_862+786dup
NM_002345.4:c.862+781_862+786dup MANE Select NP_002336.1:n.862+781_862+786dup