Canonical Allele Identifier: CA2143165703

Gene: FUT8

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65586183G= , CM000676.2:g.65586183G=	GRCh38
NC_000014.8:g.66052901G= , CM000676.1:g.66052901G=	GRCh37
NC_000014.7:g.65122654G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673929.1:c.203+24417G= MANE Select	ENSP00000501213.1:n.203+24417G=
ENST00000674118.1:c.203+24417G=	ENSP00000501008.1:n.203+24417G=
ENST00000342677.10:c.203+24417G=	ENSP00000345865.6:n.203+24417G=
ENST00000358307.6:c.-286-29795G=	ENSP00000351057.2:n.-286-29795G=
ENST00000360689.9:c.203+24417G=	ENSP00000353910.5:n.203+24417G=
ENST00000394586.6:c.203+24417G=	ENSP00000378087.2:n.203+24417G=
ENST00000557164.5:c.-286-29795G=	ENSP00000452433.1:n.-286-29795G=
NM_004480.4:c.-286-29795G=	NP_004471.4:n.-286-29795G=
NM_178155.2:c.203+24417G=	NP_835368.1:n.203+24417G=
NM_178156.2:c.203+24417G=	NP_835369.1:n.203+24417G=
NR_038167.1:n.1930+24417G=
NR_038170.1:n.1013+24417G=
XM_011536613.1:c.203+24417G=	XP_011534915.1:n.203+24417G=
XM_017021136.1:c.203+24417G=	XP_016876625.1:n.203+24417G=
XM_017021137.1:c.203+24417G=	XP_016876626.1:n.203+24417G=
XM_017021138.1:c.203+24417G=	XP_016876627.1:n.203+24417G=
XM_017021139.1:c.203+24417G=	XP_016876628.1:n.203+24417G=
XM_017021140.1:c.14+12900G=	XP_016876629.1:n.14+12900G=
NM_001371533.1:c.203+24417G= MANE Select	NP_001358462.1:n.203+24417G=
NM_001371534.1:c.203+24417G=	NP_001358463.1:n.203+24417G=
NM_001371536.1:c.203+24417G=	NP_001358465.1:n.203+24417G=
NM_178155.3:c.203+24417G=	NP_835368.1:n.203+24417G=