Canonical Allele Identifier: CA693364432

Gene: LUM

Linked Data

• dbSNP Id: rs1282790671
• MyVariant Identifiers: chr12:g.91501124_91501129del (hg19) ; chr12:g.91107347_91107352del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91107347_91107352del , CM000674.2:g.91107347_91107352del	GRCh38
NC_000012.11:g.91501124_91501129del , CM000674.1:g.91501124_91501129del	GRCh37
NC_000012.10:g.90025255_90025260del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.5:c.862+766_862+771del MANE Select	ENSP00000266718.4:n.862+766_862+771del
ENST00000266718.4:c.862+766_862+771del	ENSP00000266718.4:n.862+766_862+771del
ENST00000546642.1:n.612+766_612+771del
ENST00000548071.1:n.255+766_255+771del
NM_002345.3:c.862+766_862+771del	NP_002336.1:n.862+766_862+771del
NM_002345.4:c.862+766_862+771del MANE Select	NP_002336.1:n.862+766_862+771del