Canonical Allele Identifier: CA2054318618
Gene: LUM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107315_91107321delinsAAGAAAG , CM000674.2:g.91107315_91107321delinsAAGAAAG GRCh38
NC_000012.11:g.91501092_91501098delinsAAGAAAG , CM000674.1:g.91501092_91501098delinsAAGAAAG GRCh37
NC_000012.10:g.90025223_90025229delinsAAGAAAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+797_862+803delinsCTTTCTT MANE Select ENSP00000266718.4:n.862+797_862+803delinsCTTTCTT
ENST00000266718.4:c.862+797_862+803delinsCTTTCTT ENSP00000266718.4:n.862+797_862+803delinsCTTTCTT
ENST00000546642.1:n.612+797_612+803delinsCTTTCTT
ENST00000548071.1:n.255+797_255+803delinsCTTTCTT
NM_002345.3:c.862+797_862+803delinsCTTTCTT NP_002336.1:n.862+797_862+803delinsCTTTCTT
NM_002345.4:c.862+797_862+803delinsCTTTCTT MANE Select NP_002336.1:n.862+797_862+803delinsCTTTCTT