Canonical Allele Identifier: CA2054318660

Gene: LUM

Linked Data

• dbSNP Id: rs1880098973

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91107329_91107331del , CM000674.2:g.91107329_91107331del	GRCh38
NC_000012.11:g.91501106_91501108del , CM000674.1:g.91501106_91501108del	GRCh37
NC_000012.10:g.90025237_90025239del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.5:c.862+789_862+791del MANE Select	ENSP00000266718.4:n.862+789_862+791del
ENST00000266718.4:c.862+789_862+791del	ENSP00000266718.4:n.862+789_862+791del
ENST00000546642.1:n.612+789_612+791del
ENST00000548071.1:n.255+789_255+791del
NM_002345.3:c.862+789_862+791del	NP_002336.1:n.862+789_862+791del
NM_002345.4:c.862+789_862+791del MANE Select	NP_002336.1:n.862+789_862+791del