Canonical Allele Identifier: CA950429597
Gene: LUM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107280_91107281insGG , CM000674.2:g.91107280_91107281insGG GRCh38
NC_000012.11:g.91501057_91501058insGG , CM000674.1:g.91501057_91501058insGG GRCh37
NC_000012.10:g.90025188_90025189insGG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+837_862+838insCC MANE Select ENSP00000266718.4:n.862+837_862+838insCC
ENST00000266718.4:c.862+837_862+838insCC ENSP00000266718.4:n.862+837_862+838insCC
ENST00000546642.1:n.612+837_612+838insCC
ENST00000548071.1:n.255+837_255+838insCC
NM_002345.3:c.862+837_862+838insCC NP_002336.1:n.862+837_862+838insCC
NM_002345.4:c.862+837_862+838insCC MANE Select NP_002336.1:n.862+837_862+838insCC