Canonical Allele Identifier: CA1092128287
Gene: FUT9 HGNC NCBI

Linked Data

dbSNP Id: rs1770789007

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.96057316_96057319del , CM000668.2:g.96057316_96057319del GRCh38
NC_000006.11:g.96505192_96505195del , CM000668.1:g.96505192_96505195del GRCh37
NC_000006.10:g.96611913_96611916del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000302103.6:c.-98+41104_-98+41107del MANE Select ENSP00000302599.4:n.-98+41104_-98+41107del
ENST00000302103.5:c.-98+41104_-98+41107del ENSP00000302599.4:n.-98+41104_-98+41107del
NM_006581.3:c.-98+41104_-98+41107del NP_006572.2:n.-98+41104_-98+41107del
XM_011535384.1:c.-98+36343_-98+36346del XP_011533686.1:n.-98+36343_-98+36346del
XM_017010190.1:c.-215+41104_-215+41107del XP_016865679.1:n.-215+41104_-215+41107del
XR_001744267.2:n.1941_1944del
NM_006581.4:c.-98+41104_-98+41107del MANE Select NP_006572.2:n.-98+41104_-98+41107del