Canonical Allele Identifier: CA950428933
Gene: LUM HGNC NCBI

Linked Data

gnomAD v3: 12-91107158-A-AGAAAGAAAGAAAGAAAAC
gnomAD v4: 12-91107158-A-AGAAAGAAAGAAAGAAAAC
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107174_91107191dup , CM000674.2:g.91107174_91107191dup GRCh38
NC_000012.11:g.91500951_91500968dup , CM000674.1:g.91500951_91500968dup GRCh37
NC_000012.10:g.90025082_90025099dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000266718.5:c.862+942_862+959dup MANE Select ENSP00000266718.4:n.862+942_862+959dup
ENST00000266718.4:c.862+942_862+959dup ENSP00000266718.4:n.862+942_862+959dup
ENST00000546642.1:n.612+942_612+959dup
ENST00000548071.1:n.255+942_255+959dup
NM_002345.3:c.862+942_862+959dup NP_002336.1:n.862+942_862+959dup
NM_002345.4:c.862+942_862+959dup MANE Select NP_002336.1:n.862+942_862+959dup
Search 100 bp 5'
Search 100 bp 3'