Canonical Allele Identifier: CA2054318812
Gene: LUM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107439G= , CM000674.2:g.91107439G= GRCh38
NC_000012.11:g.91501216G= , CM000674.1:g.91501216G= GRCh37
NC_000012.10:g.90025347G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+679C= MANE Select ENSP00000266718.4:n.862+679C=
ENST00000266718.4:c.862+679C= ENSP00000266718.4:n.862+679C=
ENST00000546642.1:n.612+679C=
ENST00000548071.1:n.255+679C=
NM_002345.3:c.862+679C= NP_002336.1:n.862+679C=
NM_002345.4:c.862+679C= MANE Select NP_002336.1:n.862+679C=