Canonical Allele Identifier: CA2054318581

Gene: LUM

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91107309_91107327delinsGAAAGAAAGAAAGAAAGAA , CM000674.2:g.91107309_91107327delinsGAAAGAAAGAAAGAAAGAA	GRCh38
NC_000012.11:g.91501086_91501104delinsGAAAGAAAGAAAGAAAGAA , CM000674.1:g.91501086_91501104delinsGAAAGAAAGAAAGAAAGAA	GRCh37
NC_000012.10:g.90025217_90025235delinsGAAAGAAAGAAAGAAAGAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.5:c.862+791_862+809delinsTTCTTTCTTTCTTTCTTTC MANE Select	ENSP00000266718.4:n.862+791_862+809delinsTTCTTTCTTTCTTTCTTTC
ENST00000266718.4:c.862+791_862+809delinsTTCTTTCTTTCTTTCTTTC	ENSP00000266718.4:n.862+791_862+809delinsTTCTTTCTTTCTTTCTTTC
ENST00000546642.1:n.612+791_612+809delinsTTCTTTCTTTCTTTCTTTC
ENST00000548071.1:n.255+791_255+809delinsTTCTTTCTTTCTTTCTTTC
NM_002345.3:c.862+791_862+809delinsTTCTTTCTTTCTTTCTTTC	NP_002336.1:n.862+791_862+809delinsTTCTTTCTTTCTTTCTTTC
NM_002345.4:c.862+791_862+809delinsTTCTTTCTTTCTTTCTTTC MANE Select	NP_002336.1:n.862+791_862+809delinsTTCTTTCTTTCTTTCTTTC