Canonical Allele Identifier: CA2054318283
Gene: LUM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107247_91107248delinsGA , CM000674.2:g.91107247_91107248delinsGA GRCh38
NC_000012.11:g.91501024_91501025delinsGA , CM000674.1:g.91501024_91501025delinsGA GRCh37
NC_000012.10:g.90025155_90025156delinsGA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+870_862+871delinsTC MANE Select ENSP00000266718.4:n.862+870_862+871delinsTC
ENST00000266718.4:c.862+870_862+871delinsTC ENSP00000266718.4:n.862+870_862+871delinsTC
ENST00000546642.1:n.612+870_612+871delinsTC
ENST00000548071.1:n.255+870_255+871delinsTC
NM_002345.3:c.862+870_862+871delinsTC NP_002336.1:n.862+870_862+871delinsTC
NM_002345.4:c.862+870_862+871delinsTC MANE Select NP_002336.1:n.862+870_862+871delinsTC