Canonical Allele Identifier: CA950429864
Gene: LUM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107289_91107293del , CM000674.2:g.91107289_91107293del GRCh38
NC_000012.11:g.91501066_91501070del , CM000674.1:g.91501066_91501070del GRCh37
NC_000012.10:g.90025197_90025201del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+825_862+829del MANE Select ENSP00000266718.4:n.862+825_862+829del
ENST00000266718.4:c.862+825_862+829del ENSP00000266718.4:n.862+825_862+829del
ENST00000546642.1:n.612+825_612+829del
ENST00000548071.1:n.255+825_255+829del
NM_002345.3:c.862+825_862+829del NP_002336.1:n.862+825_862+829del
NM_002345.4:c.862+825_862+829del MANE Select NP_002336.1:n.862+825_862+829del