Canonical Allele Identifier: CA1648570687
Gene: FUT9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.96057207_96057209delinsTAA , CM000668.2:g.96057207_96057209delinsTAA GRCh38
NC_000006.11:g.96505083_96505085delinsTAA , CM000668.1:g.96505083_96505085delinsTAA GRCh37
NC_000006.10:g.96611804_96611806delinsTAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000302103.6:c.-98+40995_-98+40997delinsTAA MANE Select ENSP00000302599.4:n.-98+40995_-98+40997delinsTAA
ENST00000302103.5:c.-98+40995_-98+40997delinsTAA ENSP00000302599.4:n.-98+40995_-98+40997delinsTAA
NM_006581.3:c.-98+40995_-98+40997delinsTAA NP_006572.2:n.-98+40995_-98+40997delinsTAA
XM_011535384.1:c.-98+36234_-98+36236delinsTAA XP_011533686.1:n.-98+36234_-98+36236delinsTAA
XM_017010190.1:c.-215+40995_-215+40997delinsTAA XP_016865679.1:n.-215+40995_-215+40997delinsTAA
XR_001744267.2:n.2049_2051delinsTTA
NM_006581.4:c.-98+40995_-98+40997delinsTAA MANE Select NP_006572.2:n.-98+40995_-98+40997delinsTAA
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