Canonical Allele Identifier: CA2054318148

Gene: LUM

Linked Data

• dbSNP Id: rs1880060664

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91107216_91107217insAAAAGAAAGAAAGA , CM000674.2:g.91107216_91107217insAAAAGAAAGAAAGA	GRCh38
NC_000012.11:g.91500993_91500994insAAAAGAAAGAAAGA , CM000674.1:g.91500993_91500994insAAAAGAAAGAAAGA	GRCh37
NC_000012.10:g.90025124_90025125insAAAAGAAAGAAAGA	NCBI36

Transcript Alleles

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