Canonical Allele Identifier: CA950428748
Gene: LUM HGNC NCBI

Linked Data

gnomAD v3: 12-91107039-G-GTC
gnomAD v4: 12-91107039-G-GTC
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107039_91107040insTC , CM000674.2:g.91107039_91107040insTC GRCh38
NC_000012.11:g.91500816_91500817insTC , CM000674.1:g.91500816_91500817insTC GRCh37
NC_000012.10:g.90024947_90024948insTC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+1078_862+1079insGA MANE Select ENSP00000266718.4:n.862+1078_862+1079insGA
ENST00000266718.4:c.862+1078_862+1079insGA ENSP00000266718.4:n.862+1078_862+1079insGA
ENST00000546642.1:n.612+1078_612+1079insGA
ENST00000548071.1:n.255+1078_255+1079insGA
NM_002345.3:c.862+1078_862+1079insGA NP_002336.1:n.862+1078_862+1079insGA
NM_002345.4:c.862+1078_862+1079insGA MANE Select NP_002336.1:n.862+1078_862+1079insGA
Search 100 bp 5'
Search 100 bp 3'