Canonical Allele Identifier: CA241230240
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs879130360

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107225_91107238delinsGA , CM000674.2:g.91107225_91107238delinsGA GRCh38
NC_000012.11:g.91501002_91501015delinsGA , CM000674.1:g.91501002_91501015delinsGA GRCh37
NC_000012.10:g.90025133_90025146delinsGA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+880_862+893delinsTC MANE Select ENSP00000266718.4:n.862+880_862+893delinsTC
ENST00000266718.4:c.862+880_862+893delinsTC ENSP00000266718.4:n.862+880_862+893delinsTC
ENST00000546642.1:n.612+880_612+893delinsTC
ENST00000548071.1:n.255+880_255+893delinsTC
NM_002345.3:c.862+880_862+893delinsTC NP_002336.1:n.862+880_862+893delinsTC
NM_002345.4:c.862+880_862+893delinsTC MANE Select NP_002336.1:n.862+880_862+893delinsTC