Canonical Allele Identifier: CA2054318112

Gene: LUM

Linked Data

• dbSNP Id: rs1880058003

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91107192_91107199del , CM000674.2:g.91107192_91107199del	GRCh38
NC_000012.11:g.91500969_91500976del , CM000674.1:g.91500969_91500976del	GRCh37
NC_000012.10:g.90025100_90025107del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000266718.5:c.862+926_862+933del MANE Select	ENSP00000266718.4:n.862+926_862+933del
ENST00000266718.4:c.862+926_862+933del	ENSP00000266718.4:n.862+926_862+933del
ENST00000546642.1:n.612+926_612+933del
ENST00000548071.1:n.255+926_255+933del
NM_002345.3:c.862+926_862+933del	NP_002336.1:n.862+926_862+933del
NM_002345.4:c.862+926_862+933del MANE Select	NP_002336.1:n.862+926_862+933del