Canonical Allele Identifier: CA2054318104

Gene: LUM

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91107181_91107199delinsGAAAGAAAGAAGGAAAGAA , CM000674.2:g.91107181_91107199delinsGAAAGAAAGAAGGAAAGAA	GRCh38
NC_000012.11:g.91500958_91500976delinsGAAAGAAAGAAGGAAAGAA , CM000674.1:g.91500958_91500976delinsGAAAGAAAGAAGGAAAGAA	GRCh37
NC_000012.10:g.90025089_90025107delinsGAAAGAAAGAAGGAAAGAA	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000266718.5:c.862+919_862+937delinsTTCTTTCCTTCTTTCTTTC MANE Select	ENSP00000266718.4:n.862+919_862+937delinsTTCTTTCCTTCTTTCTTTC
ENST00000266718.4:c.862+919_862+937delinsTTCTTTCCTTCTTTCTTTC	ENSP00000266718.4:n.862+919_862+937delinsTTCTTTCCTTCTTTCTTTC
ENST00000546642.1:n.612+919_612+937delinsTTCTTTCCTTCTTTCTTTC
ENST00000548071.1:n.255+919_255+937delinsTTCTTTCCTTCTTTCTTTC
NM_002345.3:c.862+919_862+937delinsTTCTTTCCTTCTTTCTTTC	NP_002336.1:n.862+919_862+937delinsTTCTTTCCTTCTTTCTTTC
NM_002345.4:c.862+919_862+937delinsTTCTTTCCTTCTTTCTTTC MANE Select	NP_002336.1:n.862+919_862+937delinsTTCTTTCCTTCTTTCTTTC