Canonical Allele Identifier: CA2054318292
Gene: LUM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107251_91107296delinsGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAGAAAGAAA , CM000674.2:g.91107251_91107296delinsGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAGAAAGAAA GRCh38
NC_000012.11:g.91501028_91501073delinsGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAGAAAGAAA , CM000674.1:g.91501028_91501073delinsGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAGAAAGAAA GRCh37
NC_000012.10:g.90025159_90025204delinsGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAGAAAGAAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+822_862+867delinsTTTCTTTCTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTC MANE Select ENSP00000266718.4:n.862+822_862+867delinsTTTCTTTCTCTTTCTTTCTT...
ENST00000266718.4:c.862+822_862+867delinsTTTCTTTCTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTC ENSP00000266718.4:n.862+822_862+867delinsTTTCTTTCTCTTTCTTTCTT...
ENST00000546642.1:n.612+822_612+867delinsTTTCTTTCTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTC
ENST00000548071.1:n.255+822_255+867delinsTTTCTTTCTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTC
NM_002345.3:c.862+822_862+867delinsTTTCTTTCTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTC NP_002336.1:n.862+822_862+867delinsTTTCTTTCTCTTTCTTTCTTTCTTTC...
NM_002345.4:c.862+822_862+867delinsTTTCTTTCTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTC MANE Select NP_002336.1:n.862+822_862+867delinsTTTCTTTCTCTTTCTTTCTTTCTTTC...