Canonical Allele Identifier: CA693363487
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1283507429

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107198_91107199insCAAAGAAA , CM000674.2:g.91107198_91107199insCAAAGAAA GRCh38
NC_000012.11:g.91500975_91500976insCAAAGAAA , CM000674.1:g.91500975_91500976insCAAAGAAA GRCh37
NC_000012.10:g.90025106_90025107insCAAAGAAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+920_862+921insTTCTTTGT MANE Select ENSP00000266718.4:n.862+920_862+921insTTCTTTGT
ENST00000266718.4:c.862+920_862+921insTTCTTTGT ENSP00000266718.4:n.862+920_862+921insTTCTTTGT
ENST00000546642.1:n.612+920_612+921insTTCTTTGT
ENST00000548071.1:n.255+920_255+921insTTCTTTGT
NM_002345.3:c.862+920_862+921insTTCTTTGT NP_002336.1:n.862+920_862+921insTTCTTTGT
NM_002345.4:c.862+920_862+921insTTCTTTGT MANE Select NP_002336.1:n.862+920_862+921insTTCTTTGT