Canonical Allele Identifier: CA950428766

Gene: LUM

Linked Data

• gnomAD v3: 12-91107044-C-CTA
• gnomAD v4: 12-91107044-C-CTA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91107044_91107045insTA , CM000674.2:g.91107044_91107045insTA	GRCh38
NC_000012.11:g.91500821_91500822insTA , CM000674.1:g.91500821_91500822insTA	GRCh37
NC_000012.10:g.90024952_90024953insTA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.5:c.862+1073_862+1074insTA MANE Select	ENSP00000266718.4:n.862+1073_862+1074insTA
ENST00000266718.4:c.862+1073_862+1074insTA	ENSP00000266718.4:n.862+1073_862+1074insTA
ENST00000546642.1:n.612+1073_612+1074insTA
ENST00000548071.1:n.255+1073_255+1074insTA
NM_002345.3:c.862+1073_862+1074insTA	NP_002336.1:n.862+1073_862+1074insTA
NM_002345.4:c.862+1073_862+1074insTA MANE Select	NP_002336.1:n.862+1073_862+1074insTA