Canonical Allele Identifier: CA2054318451
Gene: LUM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107279_91107315delinsGAAAGAAAGAGAAAGAAAGAAAGAAAGAAAGAAAGAA , CM000674.2:g.91107279_91107315delinsGAAAGAAAGAGAAAGAAAGAAAGAAAGAAAGAAAGAA GRCh38
NC_000012.11:g.91501056_91501092delinsGAAAGAAAGAGAAAGAAAGAAAGAAAGAAAGAAAGAA , CM000674.1:g.91501056_91501092delinsGAAAGAAAGAGAAAGAAAGAAAGAAAGAAAGAAAGAA GRCh37
NC_000012.10:g.90025187_90025223delinsGAAAGAAAGAGAAAGAAAGAAAGAAAGAAAGAAAGAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+803_862+839delinsTTCTTTCTTTCTTTCTTTCTTTCTTTCTCTTTCTTTC MANE Select ENSP00000266718.4:n.862+803_862+839delinsTTCTTTCTTTCTTTCTTTCT...
ENST00000266718.4:c.862+803_862+839delinsTTCTTTCTTTCTTTCTTTCTTTCTTTCTCTTTCTTTC ENSP00000266718.4:n.862+803_862+839delinsTTCTTTCTTTCTTTCTTTCT...
ENST00000546642.1:n.612+803_612+839delinsTTCTTTCTTTCTTTCTTTCTTTCTTTCTCTTTCTTTC
ENST00000548071.1:n.255+803_255+839delinsTTCTTTCTTTCTTTCTTTCTTTCTTTCTCTTTCTTTC
NM_002345.3:c.862+803_862+839delinsTTCTTTCTTTCTTTCTTTCTTTCTTTCTCTTTCTTTC NP_002336.1:n.862+803_862+839delinsTTCTTTCTTTCTTTCTTTCTTTCTTT...
NM_002345.4:c.862+803_862+839delinsTTCTTTCTTTCTTTCTTTCTTTCTTTCTCTTTCTTTC MANE Select NP_002336.1:n.862+803_862+839delinsTTCTTTCTTTCTTTCTTTCTTTCTTT...