Canonical Allele Identifier: CA1648673510
Gene: FUT9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.96212277T= , CM000668.2:g.96212277T= GRCh38
NC_000006.11:g.96660153T= , CM000668.1:g.96660153T= GRCh37
NC_000006.10:g.96766874T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000302103.6:c.*8042T= MANE Select ENSP00000302599.4:n.*8042T=
ENST00000302103.5:c.*8042T= ENSP00000302599.4:n.*8042T=
NM_006581.3:c.*8042T= NP_006572.2:n.*8042T=
XR_942796.1:n.411-9262A=
XR_942797.1:n.218-9262A=
XR_942798.1:n.224-9262A=
XR_942799.1:n.232-9262A=
XR_942800.1:n.573-9262A=
XM_011535383.2:c.*8042T= XP_011533685.1:n.*8042T=
XM_011535385.2:c.*8042T= XP_011533687.1:n.*8042T=
XM_017010188.1:c.*8042T= XP_016865677.1:n.*8042T=
XM_017010190.1:c.*8042T= XP_016865679.1:n.*8042T=
NM_006581.4:c.*8042T= MANE Select NP_006572.2:n.*8042T=