Canonical Allele Identifier: CA2054320727
Gene: LUM HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111697_91111701delinsTTAAC , CM000674.2:g.91111697_91111701delinsTTAAC GRCh38
NC_000012.11:g.91505474_91505478delinsTTAAC , CM000674.1:g.91505474_91505478delinsTTAAC GRCh37
NC_000012.10:g.90029605_90029609delinsTTAAC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.4:c.-325_-321delinsGTTAA ENSP00000266718.4:n.-325_-321delinsGTTAA
NM_002345.3:c.-325_-321delinsGTTAA NP_002336.1:n.-325_-321delinsGTTAA
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