Canonical Allele Identifier: CA2054320742
Gene: LUM HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111724_91111727delinsAACC , CM000674.2:g.91111724_91111727delinsAACC GRCh38
NC_000012.11:g.91505501_91505504delinsAACC , CM000674.1:g.91505501_91505504delinsAACC GRCh37
NC_000012.10:g.90029632_90029635delinsAACC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.4:c.-351_-348delinsGGTT ENSP00000266718.4:n.-351_-348delinsGGTT
NM_002345.3:c.-351_-348delinsGGTT NP_002336.1:n.-351_-348delinsGGTT
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