Canonical Allele Identifier: CA2054318443
Gene: LUM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107279_91107311delinsGAAAGAAAGAGAAAGAAAGAAAGAAAGAAAGAA , CM000674.2:g.91107279_91107311delinsGAAAGAAAGAGAAAGAAAGAAAGAAAGAAAGAA GRCh38
NC_000012.11:g.91501056_91501088delinsGAAAGAAAGAGAAAGAAAGAAAGAAAGAAAGAA , CM000674.1:g.91501056_91501088delinsGAAAGAAAGAGAAAGAAAGAAAGAAAGAAAGAA GRCh37
NC_000012.10:g.90025187_90025219delinsGAAAGAAAGAGAAAGAAAGAAAGAAAGAAAGAA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000266718.5:c.862+807_862+839delinsTTCTTTCTTTCTTTCTTTCTTTCTCTTTCTTTC MANE Select ENSP00000266718.4:n.862+807_862+839delinsTTCTTTCTTTCTTTCTTTCT...
ENST00000266718.4:c.862+807_862+839delinsTTCTTTCTTTCTTTCTTTCTTTCTCTTTCTTTC ENSP00000266718.4:n.862+807_862+839delinsTTCTTTCTTTCTTTCTTTCT...
ENST00000546642.1:n.612+807_612+839delinsTTCTTTCTTTCTTTCTTTCTTTCTCTTTCTTTC
ENST00000548071.1:n.255+807_255+839delinsTTCTTTCTTTCTTTCTTTCTTTCTCTTTCTTTC
NM_002345.3:c.862+807_862+839delinsTTCTTTCTTTCTTTCTTTCTTTCTCTTTCTTTC NP_002336.1:n.862+807_862+839delinsTTCTTTCTTTCTTTCTTTCTTTCTCT...
NM_002345.4:c.862+807_862+839delinsTTCTTTCTTTCTTTCTTTCTTTCTCTTTCTTTC MANE Select NP_002336.1:n.862+807_862+839delinsTTCTTTCTTTCTTTCTTTCTTTCTCT...