Canonical Allele Identifier: CA2054318145

Gene: LUM

Linked Data

• dbSNP Id: rs1472064516

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91107210_91107211insTAAAGAAA , CM000674.2:g.91107210_91107211insTAAAGAAA	GRCh38
NC_000012.11:g.91500987_91500988insTAAAGAAA , CM000674.1:g.91500987_91500988insTAAAGAAA	GRCh37
NC_000012.10:g.90025118_90025119insTAAAGAAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.5:c.862+914_862+915insATTTCTTT MANE Select	ENSP00000266718.4:n.862+914_862+915insATTTCTTT
ENST00000266718.4:c.862+914_862+915insATTTCTTT	ENSP00000266718.4:n.862+914_862+915insATTTCTTT
ENST00000546642.1:n.612+914_612+915insATTTCTTT
ENST00000548071.1:n.255+914_255+915insATTTCTTT
NM_002345.3:c.862+914_862+915insATTTCTTT	NP_002336.1:n.862+914_862+915insATTTCTTT
NM_002345.4:c.862+914_862+915insATTTCTTT MANE Select	NP_002336.1:n.862+914_862+915insATTTCTTT