Canonical Allele Identifier: CA2054318158

Gene: LUM

Linked Data

• dbSNP Id: rs1193735600

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91107216_91107217insAAAAAAGA , CM000674.2:g.91107216_91107217insAAAAAAGA	GRCh38
NC_000012.11:g.91500993_91500994insAAAAAAGA , CM000674.1:g.91500993_91500994insAAAAAAGA	GRCh37
NC_000012.10:g.90025124_90025125insAAAAAAGA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.5:c.862+906_862+907insTTTTCTTT MANE Select	ENSP00000266718.4:n.862+906_862+907insTTTTCTTT
ENST00000266718.4:c.862+906_862+907insTTTTCTTT	ENSP00000266718.4:n.862+906_862+907insTTTTCTTT
ENST00000546642.1:n.612+906_612+907insTTTTCTTT
ENST00000548071.1:n.255+906_255+907insTTTTCTTT
NM_002345.3:c.862+906_862+907insTTTTCTTT	NP_002336.1:n.862+906_862+907insTTTTCTTT
NM_002345.4:c.862+906_862+907insTTTTCTTT MANE Select	NP_002336.1:n.862+906_862+907insTTTTCTTT