Canonical Allele Identifier: CA2054318498

Gene: LUM

Linked Data

• dbSNP Id: rs1880088169

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91107288_91107289insAT , CM000674.2:g.91107288_91107289insAT	GRCh38
NC_000012.11:g.91501065_91501066insAT , CM000674.1:g.91501065_91501066insAT	GRCh37
NC_000012.10:g.90025196_90025197insAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.5:c.862+829_862+830insAT MANE Select	ENSP00000266718.4:n.862+829_862+830insAT
ENST00000266718.4:c.862+829_862+830insAT	ENSP00000266718.4:n.862+829_862+830insAT
ENST00000546642.1:n.612+829_612+830insAT
ENST00000548071.1:n.255+829_255+830insAT
NM_002345.3:c.862+829_862+830insAT	NP_002336.1:n.862+829_862+830insAT
NM_002345.4:c.862+829_862+830insAT MANE Select	NP_002336.1:n.862+829_862+830insAT