Canonical Allele Identifier: CA2054317984
Gene: LUM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107043G= , CM000674.2:g.91107043G= GRCh38
NC_000012.11:g.91500820G= , CM000674.1:g.91500820G= GRCh37
NC_000012.10:g.90024951G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+1075C= MANE Select ENSP00000266718.4:n.862+1075C=
ENST00000266718.4:c.862+1075C= ENSP00000266718.4:n.862+1075C=
ENST00000546642.1:n.612+1075C=
ENST00000548071.1:n.255+1075C=
NM_002345.3:c.862+1075C= NP_002336.1:n.862+1075C=
NM_002345.4:c.862+1075C= MANE Select NP_002336.1:n.862+1075C=