Canonical Allele Identifier: CA2054318828
Gene: LUM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107471C= , CM000674.2:g.91107471C= GRCh38
NC_000012.11:g.91501248C= , CM000674.1:g.91501248C= GRCh37
NC_000012.10:g.90025379C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+647G= MANE Select ENSP00000266718.4:n.862+647G=
ENST00000266718.4:c.862+647G= ENSP00000266718.4:n.862+647G=
ENST00000546642.1:n.612+647G=
ENST00000548071.1:n.255+647G=
NM_002345.3:c.862+647G= NP_002336.1:n.862+647G=
NM_002345.4:c.862+647G= MANE Select NP_002336.1:n.862+647G=