Canonical Allele Identifier: CA2581617513
Gene: FUT9 HGNC NCBI

Linked Data

gnomAD v4: 6-96212238-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.96212238G>T , CM000668.2:g.96212238G>T GRCh38
NC_000006.11:g.96660114G>T , CM000668.1:g.96660114G>T GRCh37
NC_000006.10:g.96766835G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000302103.6:c.*8003G>T MANE Select ENSP00000302599.4:n.*8003G>T
ENST00000302103.5:c.*8003G>T ENSP00000302599.4:n.*8003G>T
NM_006581.3:c.*8003G>T NP_006572.2:n.*8003G>T
XR_942796.1:n.411-9223C>A
XR_942797.1:n.218-9223C>A
XR_942798.1:n.224-9223C>A
XR_942799.1:n.232-9223C>A
XR_942800.1:n.573-9223C>A
XM_011535383.2:c.*8003G>T XP_011533685.1:n.*8003G>T
XM_011535385.2:c.*8003G>T XP_011533687.1:n.*8003G>T
XM_017010188.1:c.*8003G>T XP_016865677.1:n.*8003G>T
XM_017010190.1:c.*8003G>T XP_016865679.1:n.*8003G>T
NM_006581.4:c.*8003G>T MANE Select NP_006572.2:n.*8003G>T