Canonical Allele Identifier: CA950428760
Gene: LUM HGNC NCBI

Linked Data

gnomAD v3: 12-91107042-G-GTAATCCCA
gnomAD v4: 12-91107042-G-GTAATCCCA
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107042_91107043insTAATCCCA , CM000674.2:g.91107042_91107043insTAATCCCA GRCh38
NC_000012.11:g.91500819_91500820insTAATCCCA , CM000674.1:g.91500819_91500820insTAATCCCA GRCh37
NC_000012.10:g.90024950_90024951insTAATCCCA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+1075_862+1076insTGGGATTA MANE Select ENSP00000266718.4:n.862+1075_862+1076insTGGGATTA
ENST00000266718.4:c.862+1075_862+1076insTGGGATTA ENSP00000266718.4:n.862+1075_862+1076insTGGGATTA
ENST00000546642.1:n.612+1075_612+1076insTGGGATTA
ENST00000548071.1:n.255+1075_255+1076insTGGGATTA
NM_002345.3:c.862+1075_862+1076insTGGGATTA NP_002336.1:n.862+1075_862+1076insTGGGATTA
NM_002345.4:c.862+1075_862+1076insTGGGATTA MANE Select NP_002336.1:n.862+1075_862+1076insTGGGATTA
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