Canonical Allele Identifier: CA2054320719
Gene: LUM HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111688_91111690delinsGAT , CM000674.2:g.91111688_91111690delinsGAT GRCh38
NC_000012.11:g.91505465_91505467delinsGAT , CM000674.1:g.91505465_91505467delinsGAT GRCh37
NC_000012.10:g.90029596_90029598delinsGAT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.4:c.-314_-312delinsATC ENSP00000266718.4:n.-314_-312delinsATC
NM_002345.3:c.-314_-312delinsATC NP_002336.1:n.-314_-312delinsATC
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