Canonical Allele Identifier: CA2054317962

Gene: LUM

Linked Data

• dbSNP Id: rs1725778854

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91107004_91107005insTA , CM000674.2:g.91107004_91107005insTA	GRCh38
NC_000012.11:g.91500781_91500782insTA , CM000674.1:g.91500781_91500782insTA	GRCh37
NC_000012.10:g.90024912_90024913insTA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.5:c.862+1113_862+1114insTA MANE Select	ENSP00000266718.4:n.862+1113_862+1114insTA
ENST00000266718.4:c.862+1113_862+1114insTA	ENSP00000266718.4:n.862+1113_862+1114insTA
ENST00000546642.1:n.612+1113_612+1114insTA
ENST00000548071.1:n.255+1113_255+1114insTA
NM_002345.3:c.862+1113_862+1114insTA	NP_002336.1:n.862+1113_862+1114insTA
NM_002345.4:c.862+1113_862+1114insTA MANE Select	NP_002336.1:n.862+1113_862+1114insTA