Canonical Allele Identifier: CA2054320541

Gene: LUM

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91111351T= , CM000674.2:g.91111351T=	GRCh38
NC_000012.11:g.91505128T= , CM000674.1:g.91505128T=	GRCh37
NC_000012.10:g.90029259T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.5:c.-22+47A= MANE Select	ENSP00000266718.4:n.-22+47A=
ENST00000266718.4:c.-22+47A=	ENSP00000266718.4:n.-22+47A=
ENST00000546642.1:n.42+47A=
ENST00000548071.1:n.89+47A=
NM_002345.3:c.-22+47A=	NP_002336.1:n.-22+47A=
NM_002345.4:c.-22+47A= MANE Select	NP_002336.1:n.-22+47A=