Canonical Allele Identifier: CA2054318342

Gene: LUM

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91107259_91107265delinsGAAAGAA , CM000674.2:g.91107259_91107265delinsGAAAGAA	GRCh38
NC_000012.11:g.91501036_91501042delinsGAAAGAA , CM000674.1:g.91501036_91501042delinsGAAAGAA	GRCh37
NC_000012.10:g.90025167_90025173delinsGAAAGAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.5:c.862+853_862+859delinsTTCTTTC MANE Select	ENSP00000266718.4:n.862+853_862+859delinsTTCTTTC
ENST00000266718.4:c.862+853_862+859delinsTTCTTTC	ENSP00000266718.4:n.862+853_862+859delinsTTCTTTC
ENST00000546642.1:n.612+853_612+859delinsTTCTTTC
ENST00000548071.1:n.255+853_255+859delinsTTCTTTC
NM_002345.3:c.862+853_862+859delinsTTCTTTC	NP_002336.1:n.862+853_862+859delinsTTCTTTC
NM_002345.4:c.862+853_862+859delinsTTCTTTC MANE Select	NP_002336.1:n.862+853_862+859delinsTTCTTTC