Canonical Allele Identifier: CA241230060

Gene: LUM

Linked Data

• dbSNP Id: rs1028527747
• MyVariant Identifiers: chr12:g.91500847_91500848insG (hg19) ; chr12:g.91107070_91107071insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91107076dup , CM000674.2:g.91107076dup	GRCh38
NC_000012.11:g.91500853dup , CM000674.1:g.91500853dup	GRCh37
NC_000012.10:g.90024984dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.5:c.862+1047dup MANE Select	ENSP00000266718.4:n.862+1047dup
ENST00000266718.4:c.862+1047dup	ENSP00000266718.4:n.862+1047dup
ENST00000546642.1:n.612+1047dup
ENST00000548071.1:n.255+1047dup
NM_002345.3:c.862+1047dup	NP_002336.1:n.862+1047dup
NM_002345.4:c.862+1047dup MANE Select	NP_002336.1:n.862+1047dup