Canonical Allele Identifier: CA2054318188
Gene: LUM HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107221A= , CM000674.2:g.91107221A= GRCh38
NC_000012.11:g.91500998A= , CM000674.1:g.91500998A= GRCh37
NC_000012.10:g.90025129A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+897T= MANE Select ENSP00000266718.4:n.862+897T=
ENST00000266718.4:c.862+897T= ENSP00000266718.4:n.862+897T=
ENST00000546642.1:n.612+897T=
ENST00000548071.1:n.255+897T=
NM_002345.3:c.862+897T= NP_002336.1:n.862+897T=
NM_002345.4:c.862+897T= MANE Select NP_002336.1:n.862+897T=
Search 100 bp 5'
Search 100 bp 3'