Canonical Allele Identifier: CA2054318834
Gene: LUM HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107495T= , CM000674.2:g.91107495T= GRCh38
NC_000012.11:g.91501272T= , CM000674.1:g.91501272T= GRCh37
NC_000012.10:g.90025403T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000266718.5:c.862+623A= MANE Select ENSP00000266718.4:n.862+623A=
ENST00000266718.4:c.862+623A= ENSP00000266718.4:n.862+623A=
ENST00000546642.1:n.612+623A=
ENST00000548071.1:n.255+623A=
NM_002345.3:c.862+623A= NP_002336.1:n.862+623A=
NM_002345.4:c.862+623A= MANE Select NP_002336.1:n.862+623A=
Search 100 bp 5'
Search 100 bp 3'