Canonical Allele Identifier: CA2054318831
Gene: LUM HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107482_91107483delinsCA , CM000674.2:g.91107482_91107483delinsCA GRCh38
NC_000012.11:g.91501259_91501260delinsCA , CM000674.1:g.91501259_91501260delinsCA GRCh37
NC_000012.10:g.90025390_90025391delinsCA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+635_862+636delinsTG MANE Select ENSP00000266718.4:n.862+635_862+636delinsTG
ENST00000266718.4:c.862+635_862+636delinsTG ENSP00000266718.4:n.862+635_862+636delinsTG
ENST00000546642.1:n.612+635_612+636delinsTG
ENST00000548071.1:n.255+635_255+636delinsTG
NM_002345.3:c.862+635_862+636delinsTG NP_002336.1:n.862+635_862+636delinsTG
NM_002345.4:c.862+635_862+636delinsTG MANE Select NP_002336.1:n.862+635_862+636delinsTG
Search 100 bp 5'
Search 100 bp 3'