Canonical Allele Identifier: CA2054318471
Gene: LUM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107283_91107323delinsGAAAGAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA , CM000674.2:g.91107283_91107323delinsGAAAGAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA GRCh38
NC_000012.11:g.91501060_91501100delinsGAAAGAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA , CM000674.1:g.91501060_91501100delinsGAAAGAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA GRCh37
NC_000012.10:g.90025191_90025231delinsGAAAGAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000266718.5:c.862+795_862+835delinsTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTCTTTC MANE Select ENSP00000266718.4:n.862+795_862+835delins...
ENST00000266718.4:c.862+795_862+835delinsTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTCTTTC ENSP00000266718.4:n.862+795_862+835delins...
ENST00000546642.1:n.612+795_612+835delinsTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTCTTTC
ENST00000548071.1:n.255+795_255+835delinsTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTCTTTC
NM_002345.3:c.862+795_862+835delinsTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTCTTTC NP_002336.1:n.862+795_862+835delinsTTCTTT...
NM_002345.4:c.862+795_862+835delinsTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTCTTTC MANE Select NP_002336.1:n.862+795_862+835delinsTTCTTT...