Canonical Allele Identifier: CA481083471

Gene: LUM

Linked Data

• MyVariant Identifiers: chr12:g.91501021_91501022insG (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91107244_91107245insG , CM000674.2:g.91107244_91107245insG	GRCh38
NC_000012.11:g.91501021_91501022insG , CM000674.1:g.91501021_91501022insG	GRCh37
NC_000012.10:g.90025152_90025153insG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.5:c.862+873_862+874insC MANE Select	ENSP00000266718.4:n.862+873_862+874insC
ENST00000266718.4:c.862+873_862+874insC	ENSP00000266718.4:n.862+873_862+874insC
ENST00000546642.1:n.612+873_612+874insC
ENST00000548071.1:n.255+873_255+874insC
NM_002345.3:c.862+873_862+874insC	NP_002336.1:n.862+873_862+874insC
NM_002345.4:c.862+873_862+874insC MANE Select	NP_002336.1:n.862+873_862+874insC