Canonical Allele Identifier: CA2054320568
Gene: LUM HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111401A= , CM000674.2:g.91111401A= GRCh38
NC_000012.11:g.91505178A= , CM000674.1:g.91505178A= GRCh37
NC_000012.10:g.90029309A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.-25T= MANE Select ENSP00000266718.4:n.-25T=
ENST00000266718.4:c.-25T= ENSP00000266718.4:n.-25T=
ENST00000546642.1:n.39T=
ENST00000548071.1:n.86T=
NM_002345.3:c.-25T= NP_002336.1:n.-25T=
NM_002345.4:c.-25T= MANE Select NP_002336.1:n.-25T=
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