Canonical Allele Identifier: CA2054318423
Gene: LUM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107275_91107323delinsGAAAGAAAGAAAGAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA , CM000674.2:g.91107275_91107323delinsGAAAGAAAGAAAGAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA GRCh38
NC_000012.11:g.91501052_91501100delinsGAAAGAAAGAAAGAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA , CM000674.1:g.91501052_91501100delinsGAAAGAAAGAAAGAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA GRCh37
NC_000012.10:g.90025183_90025231delinsGAAAGAAAGAAAGAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000266718.5:c.862+795_862+843delinsTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTCTTTCTTTCTTTC MANE Select ENSP00000266718.4:n.862+795_862+843delins...
ENST00000266718.4:c.862+795_862+843delinsTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTCTTTCTTTCTTTC ENSP00000266718.4:n.862+795_862+843delins...
ENST00000546642.1:n.612+795_612+843delinsTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTCTTTCTTTCTTTC
ENST00000548071.1:n.255+795_255+843delinsTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTCTTTCTTTCTTTC
NM_002345.3:c.862+795_862+843delinsTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTCTTTCTTTCTTTC NP_002336.1:n.862+795_862+843delinsTTCTTT...
NM_002345.4:c.862+795_862+843delinsTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTCTTTCTTTCTTTC MANE Select NP_002336.1:n.862+795_862+843delinsTTCTTT...