Canonical Allele Identifier: CA693363631

Gene: LUM

Linked Data

• dbSNP Id: rs1491268903
• MyVariant Identifiers: chr12:g.91501012_91501013insAG (hg19) ; chr12:g.91107235_91107236insAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91107236_91107237insGA , CM000674.2:g.91107236_91107237insGA	GRCh38
NC_000012.11:g.91501013_91501014insGA , CM000674.1:g.91501013_91501014insGA	GRCh37
NC_000012.10:g.90025144_90025145insGA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.5:c.862+882_862+883insCT MANE Select	ENSP00000266718.4:n.862+882_862+883insCT
ENST00000266718.4:c.862+882_862+883insCT	ENSP00000266718.4:n.862+882_862+883insCT
ENST00000546642.1:n.612+882_612+883insCT
ENST00000548071.1:n.255+882_255+883insCT
NM_002345.3:c.862+882_862+883insCT	NP_002336.1:n.862+882_862+883insCT
NM_002345.4:c.862+882_862+883insCT MANE Select	NP_002336.1:n.862+882_862+883insCT