Canonical Allele Identifier: CA2054318192
Gene: LUM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107223_91107227delinsGAAGA , CM000674.2:g.91107223_91107227delinsGAAGA GRCh38
NC_000012.11:g.91501000_91501004delinsGAAGA , CM000674.1:g.91501000_91501004delinsGAAGA GRCh37
NC_000012.10:g.90025131_90025135delinsGAAGA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+891_862+895delinsTCTTC MANE Select ENSP00000266718.4:n.862+891_862+895delinsTCTTC
ENST00000266718.4:c.862+891_862+895delinsTCTTC ENSP00000266718.4:n.862+891_862+895delinsTCTTC
ENST00000546642.1:n.612+891_612+895delinsTCTTC
ENST00000548071.1:n.255+891_255+895delinsTCTTC
NM_002345.3:c.862+891_862+895delinsTCTTC NP_002336.1:n.862+891_862+895delinsTCTTC
NM_002345.4:c.862+891_862+895delinsTCTTC MANE Select NP_002336.1:n.862+891_862+895delinsTCTTC