Canonical Allele Identifier: CA2054318128

Gene: LUM

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91107191_91107197delinsAGGAAAG , CM000674.2:g.91107191_91107197delinsAGGAAAG	GRCh38
NC_000012.11:g.91500968_91500974delinsAGGAAAG , CM000674.1:g.91500968_91500974delinsAGGAAAG	GRCh37
NC_000012.10:g.90025099_90025105delinsAGGAAAG	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000266718.5:c.862+921_862+927delinsCTTTCCT MANE Select	ENSP00000266718.4:n.862+921_862+927delinsCTTTCCT
ENST00000266718.4:c.862+921_862+927delinsCTTTCCT	ENSP00000266718.4:n.862+921_862+927delinsCTTTCCT
ENST00000546642.1:n.612+921_612+927delinsCTTTCCT
ENST00000548071.1:n.255+921_255+927delinsCTTTCCT
NM_002345.3:c.862+921_862+927delinsCTTTCCT	NP_002336.1:n.862+921_862+927delinsCTTTCCT
NM_002345.4:c.862+921_862+927delinsCTTTCCT MANE Select	NP_002336.1:n.862+921_862+927delinsCTTTCCT