Canonical Allele Identifier: CA2726856064

Gene: LUM

Linked Data

• dbSNP Id: rs2121048563

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91107318_91107350del , CM000674.2:g.91107318_91107350del	GRCh38
NC_000012.11:g.91501095_91501127del , CM000674.1:g.91501095_91501127del	GRCh37
NC_000012.10:g.90025226_90025258del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.5:c.862+768_862+800del MANE Select	ENSP00000266718.4:n.862+768_862+800del
ENST00000266718.4:c.862+768_862+800del	ENSP00000266718.4:n.862+768_862+800del
ENST00000546642.1:n.612+768_612+800del
ENST00000548071.1:n.255+768_255+800del
NM_002345.3:c.862+768_862+800del	NP_002336.1:n.862+768_862+800del
NM_002345.4:c.862+768_862+800del MANE Select	NP_002336.1:n.862+768_862+800del