Canonical Allele Identifier: CA2600912206
Gene: LUM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107212_91107213insGAGAAAG , CM000674.2:g.91107212_91107213insGAGAAAG GRCh38
NC_000012.11:g.91500989_91500990insGAGAAAG , CM000674.1:g.91500989_91500990insGAGAAAG GRCh37
NC_000012.10:g.90025120_90025121insGAGAAAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+905_862+906insCTTTCTC MANE Select ENSP00000266718.4:n.862+905_862+906insCTTTCTC
ENST00000266718.4:c.862+905_862+906insCTTTCTC ENSP00000266718.4:n.862+905_862+906insCTTTCTC
ENST00000546642.1:n.612+905_612+906insCTTTCTC
ENST00000548071.1:n.255+905_255+906insCTTTCTC
NM_002345.3:c.862+905_862+906insCTTTCTC NP_002336.1:n.862+905_862+906insCTTTCTC
NM_002345.4:c.862+905_862+906insCTTTCTC MANE Select NP_002336.1:n.862+905_862+906insCTTTCTC