Canonical Allele Identifier: CA693363855

Gene: LUM

Linked Data

• dbSNP Id: rs1362955981
• MyVariant Identifiers: chr12:g.91501041_91501046del (hg19) ; chr12:g.91107264_91107269del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91107265_91107270del , CM000674.2:g.91107265_91107270del	GRCh38
NC_000012.11:g.91501042_91501047del , CM000674.1:g.91501042_91501047del	GRCh37
NC_000012.10:g.90025173_90025178del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.5:c.862+849_862+854del MANE Select	ENSP00000266718.4:n.862+849_862+854del
ENST00000266718.4:c.862+849_862+854del	ENSP00000266718.4:n.862+849_862+854del
ENST00000546642.1:n.612+849_612+854del
ENST00000548071.1:n.255+849_255+854del
NM_002345.3:c.862+849_862+854del	NP_002336.1:n.862+849_862+854del
NM_002345.4:c.862+849_862+854del MANE Select	NP_002336.1:n.862+849_862+854del