Canonical Allele Identifier: CA2511443663

Gene: LUM

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91107335A>G , CM000674.2:g.91107335A>G	GRCh38
NC_000012.11:g.91501112A>G , CM000674.1:g.91501112A>G	GRCh37
NC_000012.10:g.90025243A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.5:c.862+783T>C MANE Select	ENSP00000266718.4:n.862+783T>C
ENST00000266718.4:c.862+783T>C	ENSP00000266718.4:n.862+783T>C
ENST00000546642.1:n.612+783T>C
ENST00000548071.1:n.255+783T>C
NM_002345.3:c.862+783T>C	NP_002336.1:n.862+783T>C
NM_002345.4:c.862+783T>C MANE Select	NP_002336.1:n.862+783T>C