Canonical Allele Identifier: CA950429710
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs869096187

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107330_91107345dup , CM000674.2:g.91107330_91107345dup GRCh38
NC_000012.11:g.91501107_91501122dup , CM000674.1:g.91501107_91501122dup GRCh37
NC_000012.10:g.90025238_90025253dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000266718.5:c.862+815_862+830dup MANE Select ENSP00000266718.4:n.862+815_862+830dup
ENST00000266718.4:c.862+815_862+830dup ENSP00000266718.4:n.862+815_862+830dup
ENST00000546642.1:n.612+815_612+830dup
ENST00000548071.1:n.255+815_255+830dup
NM_002345.3:c.862+815_862+830dup NP_002336.1:n.862+815_862+830dup
NM_002345.4:c.862+815_862+830dup MANE Select NP_002336.1:n.862+815_862+830dup