Canonical Allele Identifier: CA1648570738

Gene: FUT9

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.96057327_96057330delinsCTTT , CM000668.2:g.96057327_96057330delinsCTTT	GRCh38
NC_000006.11:g.96505203_96505206delinsCTTT , CM000668.1:g.96505203_96505206delinsCTTT	GRCh37
NC_000006.10:g.96611924_96611927delinsCTTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302103.6:c.-98+41115_-98+41118delinsCTTT MANE Select	ENSP00000302599.4:n.-98+41115_-98+41118delinsCTTT
ENST00000302103.5:c.-98+41115_-98+41118delinsCTTT	ENSP00000302599.4:n.-98+41115_-98+41118delinsCTTT
NM_006581.3:c.-98+41115_-98+41118delinsCTTT	NP_006572.2:n.-98+41115_-98+41118delinsCTTT
XM_011535384.1:c.-98+36354_-98+36357delinsCTTT	XP_011533686.1:n.-98+36354_-98+36357delinsCTTT
XM_017010190.1:c.-215+41115_-215+41118delinsCTTT	XP_016865679.1:n.-215+41115_-215+41118delinsCTTT
XR_001744267.2:n.1928_1931delinsAAAG
NM_006581.4:c.-98+41115_-98+41118delinsCTTT MANE Select	NP_006572.2:n.-98+41115_-98+41118delinsCTTT