Canonical Allele Identifier: CA2054317988

Gene: LUM

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91107051T= , CM000674.2:g.91107051T=	GRCh38
NC_000012.11:g.91500828T= , CM000674.1:g.91500828T=	GRCh37
NC_000012.10:g.90024959T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.5:c.862+1067A= MANE Select	ENSP00000266718.4:n.862+1067A=
ENST00000266718.4:c.862+1067A=	ENSP00000266718.4:n.862+1067A=
ENST00000546642.1:n.612+1067A=
ENST00000548071.1:n.255+1067A=
NM_002345.3:c.862+1067A=	NP_002336.1:n.862+1067A=
NM_002345.4:c.862+1067A= MANE Select	NP_002336.1:n.862+1067A=