Canonical Allele Identifier: CA2054318101
Gene: LUM HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107180_91107181delinsAG , CM000674.2:g.91107180_91107181delinsAG GRCh38
NC_000012.11:g.91500957_91500958delinsAG , CM000674.1:g.91500957_91500958delinsAG GRCh37
NC_000012.10:g.90025088_90025089delinsAG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000266718.5:c.862+937_862+938delinsCT MANE Select ENSP00000266718.4:n.862+937_862+938delinsCT
ENST00000266718.4:c.862+937_862+938delinsCT ENSP00000266718.4:n.862+937_862+938delinsCT
ENST00000546642.1:n.612+937_612+938delinsCT
ENST00000548071.1:n.255+937_255+938delinsCT
NM_002345.3:c.862+937_862+938delinsCT NP_002336.1:n.862+937_862+938delinsCT
NM_002345.4:c.862+937_862+938delinsCT MANE Select NP_002336.1:n.862+937_862+938delinsCT
Search 100 bp 5'
Search 100 bp 3'