Canonical Allele Identifier: CA1648638187

Gene: FUT9

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.96111973C= , CM000668.2:g.96111973C=	GRCh38
NC_000006.11:g.96559849C= , CM000668.1:g.96559849C=	GRCh37
NC_000006.10:g.96666570C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_006581.4:c.-97-2066C= MANE Select	NP_006572.2:n.-97-2066C=
ENST00000302103.6:c.-97-2066C= MANE Select	ENSP00000302599.4:n.-97-2066C=
NM_006581.3:c.-97-2066C=	NP_006572.2:n.-97-2066C=
ENST00000302103.5:c.-97-2066C=	ENSP00000302599.4:n.-97-2066C=
XM_011535383.1:c.-98+1175C=	XP_011533685.1:n.-98+1175C=
XM_011535383.2:c.-98+1175C=	XP_011533685.1:n.-98+1175C=
XM_011535384.1:c.-97-2066C=	XP_011533686.1:n.-97-2066C=
XM_011535385.1:c.-215+1175C=	XP_011533687.1:n.-215+1175C=
XM_011535385.2:c.-215+1175C=	XP_011533687.1:n.-215+1175C=
XM_017010188.1:c.-98+1175C=	XP_016865677.1:n.-98+1175C=
XM_017010190.1:c.-214-2066C=	XP_016865679.1:n.-214-2066C=