Canonical Allele Identifier: CA1648570796
Gene: FUT9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.96057455_96057459delinsCAGAA , CM000668.2:g.96057455_96057459delinsCAGAA GRCh38
NC_000006.11:g.96505331_96505335delinsCAGAA , CM000668.1:g.96505331_96505335delinsCAGAA GRCh37
NC_000006.10:g.96612052_96612056delinsCAGAA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000302103.6:c.-98+41243_-98+41247delinsCAGAA MANE Select ENSP00000302599.4:n.-98+41243_-98+41247delinsCAGAA
ENST00000302103.5:c.-98+41243_-98+41247delinsCAGAA ENSP00000302599.4:n.-98+41243_-98+41247delinsCAGAA
NM_006581.3:c.-98+41243_-98+41247delinsCAGAA NP_006572.2:n.-98+41243_-98+41247delinsCAGAA
XM_011535384.1:c.-98+36482_-98+36486delinsCAGAA XP_011533686.1:n.-98+36482_-98+36486delinsCAGAA
XM_017010190.1:c.-215+41243_-215+41247delinsCAGAA XP_016865679.1:n.-215+41243_-215+41247delinsCAGAA
XR_001744267.2:n.1799_1803delinsTTCTG
NM_006581.4:c.-98+41243_-98+41247delinsCAGAA MANE Select NP_006572.2:n.-98+41243_-98+41247delinsCAGAA