Canonical Allele Identifier: CA2796947663

Gene: LUM

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91107276_91107277insG , CM000674.2:g.91107276_91107277insG	GRCh38
NC_000012.11:g.91501053_91501054insG , CM000674.1:g.91501053_91501054insG	GRCh37
NC_000012.10:g.90025184_90025185insG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.5:c.862+841_862+842insC MANE Select	ENSP00000266718.4:n.862+841_862+842insC
ENST00000266718.4:c.862+841_862+842insC	ENSP00000266718.4:n.862+841_862+842insC
ENST00000546642.1:n.612+841_612+842insC
ENST00000548071.1:n.255+841_255+842insC
NM_002345.3:c.862+841_862+842insC	NP_002336.1:n.862+841_862+842insC
NM_002345.4:c.862+841_862+842insC MANE Select	NP_002336.1:n.862+841_862+842insC