Canonical Allele Identifier: CA2620150150
Gene: LUM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111381_91111382insATG , CM000674.2:g.91111381_91111382insATG GRCh38
NC_000012.11:g.91505158_91505159insATG , CM000674.1:g.91505158_91505159insATG GRCh37
NC_000012.10:g.90029289_90029290insATG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.-22+17_-22+18insATC MANE Select ENSP00000266718.4:n.-22+17_-22+18insATC
ENST00000266718.4:c.-22+17_-22+18insATC ENSP00000266718.4:n.-22+17_-22+18insATC
ENST00000546642.1:n.42+17_42+18insATC
ENST00000548071.1:n.89+17_89+18insATC
NM_002345.3:c.-22+17_-22+18insATC NP_002336.1:n.-22+17_-22+18insATC
NM_002345.4:c.-22+17_-22+18insATC MANE Select NP_002336.1:n.-22+17_-22+18insATC