Canonical Allele Identifier: CA2054318398
Gene: LUM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107271_91107299delinsGAAAGAAAGAAAGAAAGAGAAAGAAAGAA , CM000674.2:g.91107271_91107299delinsGAAAGAAAGAAAGAAAGAGAAAGAAAGAA GRCh38
NC_000012.11:g.91501048_91501076delinsGAAAGAAAGAAAGAAAGAGAAAGAAAGAA , CM000674.1:g.91501048_91501076delinsGAAAGAAAGAAAGAAAGAGAAAGAAAGAA GRCh37
NC_000012.10:g.90025179_90025207delinsGAAAGAAAGAAAGAAAGAGAAAGAAAGAA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000266718.5:c.862+819_862+847delinsTTCTTTCTTTCTCTTTCTTTCTTTCTTTC MANE Select ENSP00000266718.4:n.862+819_862+847delinsTTCTTTCTTTCTCTTTCTTT...
ENST00000266718.4:c.862+819_862+847delinsTTCTTTCTTTCTCTTTCTTTCTTTCTTTC ENSP00000266718.4:n.862+819_862+847delinsTTCTTTCTTTCTCTTTCTTT...
ENST00000546642.1:n.612+819_612+847delinsTTCTTTCTTTCTCTTTCTTTCTTTCTTTC
ENST00000548071.1:n.255+819_255+847delinsTTCTTTCTTTCTCTTTCTTTCTTTCTTTC
NM_002345.3:c.862+819_862+847delinsTTCTTTCTTTCTCTTTCTTTCTTTCTTTC NP_002336.1:n.862+819_862+847delinsTTCTTTCTTTCTCTTTCTTTCTTTCT...
NM_002345.4:c.862+819_862+847delinsTTCTTTCTTTCTCTTTCTTTCTTTCTTTC MANE Select NP_002336.1:n.862+819_862+847delinsTTCTTTCTTTCTCTTTCTTTCTTTCT...