Canonical Allele Identifier: CA693363514
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1555188571

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107202_91107203insAGAAA , CM000674.2:g.91107202_91107203insAGAAA GRCh38
NC_000012.11:g.91500979_91500980insAGAAA , CM000674.1:g.91500979_91500980insAGAAA GRCh37
NC_000012.10:g.90025110_90025111insAGAAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+918_862+919insCTTTT MANE Select ENSP00000266718.4:n.862+918_862+919insCTTTT
ENST00000266718.4:c.862+918_862+919insCTTTT ENSP00000266718.4:n.862+918_862+919insCTTTT
ENST00000546642.1:n.612+918_612+919insCTTTT
ENST00000548071.1:n.255+918_255+919insCTTTT
NM_002345.3:c.862+918_862+919insCTTTT NP_002336.1:n.862+918_862+919insCTTTT
NM_002345.4:c.862+918_862+919insCTTTT MANE Select NP_002336.1:n.862+918_862+919insCTTTT