Canonical Allele Identifier: CA2054320533

Gene: LUM

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91111336T= , CM000674.2:g.91111336T=	GRCh38
NC_000012.11:g.91505113T= , CM000674.1:g.91505113T=	GRCh37
NC_000012.10:g.90029244T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.5:c.-22+62A= MANE Select	ENSP00000266718.4:n.-22+62A=
ENST00000266718.4:c.-22+62A=	ENSP00000266718.4:n.-22+62A=
ENST00000546642.1:n.42+62A=
ENST00000548071.1:n.89+62A=
NM_002345.3:c.-22+62A=	NP_002336.1:n.-22+62A=
NM_002345.4:c.-22+62A= MANE Select	NP_002336.1:n.-22+62A=