Canonical Allele Identifier: CA2054318682
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1491579475

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107333_91107334dup , CM000674.2:g.91107333_91107334dup GRCh38
NC_000012.11:g.91501110_91501111dup , CM000674.1:g.91501110_91501111dup GRCh37
NC_000012.10:g.90025241_90025242dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000266718.5:c.862+785_862+786dup MANE Select ENSP00000266718.4:n.862+785_862+786dup
ENST00000266718.4:c.862+785_862+786dup ENSP00000266718.4:n.862+785_862+786dup
ENST00000546642.1:n.612+785_612+786dup
ENST00000548071.1:n.255+785_255+786dup
NM_002345.3:c.862+785_862+786dup NP_002336.1:n.862+785_862+786dup
NM_002345.4:c.862+785_862+786dup MANE Select NP_002336.1:n.862+785_862+786dup