Canonical Allele Identifier: CA2054318170

Gene: LUM

Linked Data

• dbSNP Id: rs1489011765

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91107216_91107217insAAGACAGA , CM000674.2:g.91107216_91107217insAAGACAGA	GRCh38
NC_000012.11:g.91500993_91500994insAAGACAGA , CM000674.1:g.91500993_91500994insAAGACAGA	GRCh37
NC_000012.10:g.90025124_90025125insAAGACAGA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.5:c.862+904_862+905insGTCTTTCT MANE Select	ENSP00000266718.4:n.862+904_862+905insGTCTTTCT
ENST00000266718.4:c.862+904_862+905insGTCTTTCT	ENSP00000266718.4:n.862+904_862+905insGTCTTTCT
ENST00000546642.1:n.612+904_612+905insGTCTTTCT
ENST00000548071.1:n.255+904_255+905insGTCTTTCT
NM_002345.3:c.862+904_862+905insGTCTTTCT	NP_002336.1:n.862+904_862+905insGTCTTTCT
NM_002345.4:c.862+904_862+905insGTCTTTCT MANE Select	NP_002336.1:n.862+904_862+905insGTCTTTCT