Canonical Allele Identifier: CA1648570739
Gene: FUT9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.96057327_96057331delinsCTTTA , CM000668.2:g.96057327_96057331delinsCTTTA GRCh38
NC_000006.11:g.96505203_96505207delinsCTTTA , CM000668.1:g.96505203_96505207delinsCTTTA GRCh37
NC_000006.10:g.96611924_96611928delinsCTTTA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000302103.6:c.-98+41115_-98+41119delinsCTTTA MANE Select ENSP00000302599.4:n.-98+41115_-98+41119delinsCTTTA
ENST00000302103.5:c.-98+41115_-98+41119delinsCTTTA ENSP00000302599.4:n.-98+41115_-98+41119delinsCTTTA
NM_006581.3:c.-98+41115_-98+41119delinsCTTTA NP_006572.2:n.-98+41115_-98+41119delinsCTTTA
XM_011535384.1:c.-98+36354_-98+36358delinsCTTTA XP_011533686.1:n.-98+36354_-98+36358delinsCTTTA
XM_017010190.1:c.-215+41115_-215+41119delinsCTTTA XP_016865679.1:n.-215+41115_-215+41119delinsCTTTA
XR_001744267.2:n.1927_1931delinsTAAAG
NM_006581.4:c.-98+41115_-98+41119delinsCTTTA MANE Select NP_006572.2:n.-98+41115_-98+41119delinsCTTTA