Canonical Allele Identifier: CA2054320668
Gene: LUM HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111574_91111576delinsTTA , CM000674.2:g.91111574_91111576delinsTTA GRCh38
NC_000012.11:g.91505351_91505353delinsTTA , CM000674.1:g.91505351_91505353delinsTTA GRCh37
NC_000012.10:g.90029482_90029484delinsTTA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.4:c.-200_-198delinsTAA ENSP00000266718.4:n.-200_-198delinsTAA
NM_002345.3:c.-200_-198delinsTAA NP_002336.1:n.-200_-198delinsTAA
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