Canonical Allele Identifier: CA2054318143

Gene: LUM

Linked Data

• dbSNP Id: rs1880060451

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91107202A>C , CM000674.2:g.91107202A>C	GRCh38
NC_000012.11:g.91500979A>C , CM000674.1:g.91500979A>C	GRCh37
NC_000012.10:g.90025110A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000266718.5:c.862+916T>G MANE Select	ENSP00000266718.4:n.862+916T>G
ENST00000266718.4:c.862+916T>G	ENSP00000266718.4:n.862+916T>G
ENST00000546642.1:n.612+916T>G
ENST00000548071.1:n.255+916T>G
NM_002345.3:c.862+916T>G	NP_002336.1:n.862+916T>G
NM_002345.4:c.862+916T>G MANE Select	NP_002336.1:n.862+916T>G