Canonical Allele Identifier: CA2054318321
Gene: LUM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107255_91107300delinsGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAGAAAGAAAGAAA , CM000674.2:g.91107255_91107300delinsGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAGAAAGAAAGAAA GRCh38
NC_000012.11:g.91501032_91501077delinsGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAGAAAGAAAGAAA , CM000674.1:g.91501032_91501077delinsGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAGAAAGAAAGAAA GRCh37
NC_000012.10:g.90025163_90025208delinsGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAGAAAGAAAGAAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+818_862+863delinsTTTCTTTCTTTCTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTC MANE Select ENSP00000266718.4:n.862+818_862+863delinsTTTCTTTCTTTCTCTTTCTT...
ENST00000266718.4:c.862+818_862+863delinsTTTCTTTCTTTCTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTC ENSP00000266718.4:n.862+818_862+863delinsTTTCTTTCTTTCTCTTTCTT...
ENST00000546642.1:n.612+818_612+863delinsTTTCTTTCTTTCTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTC
ENST00000548071.1:n.255+818_255+863delinsTTTCTTTCTTTCTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTC
NM_002345.3:c.862+818_862+863delinsTTTCTTTCTTTCTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTC NP_002336.1:n.862+818_862+863delinsTTTCTTTCTTTCTCTTTCTTTCTTTC...
NM_002345.4:c.862+818_862+863delinsTTTCTTTCTTTCTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTC MANE Select NP_002336.1:n.862+818_862+863delinsTTTCTTTCTTTCTCTTTCTTTCTTTC...