Canonical Allele Identifier: CA2143138295

Gene: FUT8

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65471009G= , CM000676.2:g.65471009G=	GRCh38
NC_000014.8:g.65937727G= , CM000676.1:g.65937727G=	GRCh37
NC_000014.7:g.65007480G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000673929.1:c.-228+15291G= MANE Select	ENSP00000501213.1:n.-228+15291G=
ENST00000674118.1:c.-228+15291G=	ENSP00000501008.1:n.-228+15291G=
ENST00000342677.10:c.-228+15291G=	ENSP00000345865.6:n.-228+15291G=
ENST00000358307.6:c.-287+15291G=	ENSP00000351057.2:n.-287+15291G=
ENST00000360689.9:c.-228+15291G=	ENSP00000353910.5:n.-228+15291G=
ENST00000394586.6:c.-228+59016G=	ENSP00000378087.2:n.-228+59016G=
ENST00000553924.5:c.-374+15291G=	ENSP00000451577.1:n.-374+15291G=
ENST00000554610.1:c.-228+57795G=	ENSP00000452309.1:n.-228+57795G=
ENST00000555559.5:c.-305-8698G=	ENSP00000451689.1:n.-305-8698G=
ENST00000556518.5:c.-228+15291G=	ENSP00000452597.1:n.-228+15291G=
ENST00000557164.5:c.-287+15291G=	ENSP00000452433.1:n.-287+15291G=
ENST00000557338.5:c.-305-8698G=	ENSP00000452105.1:n.-305-8698G=
NM_004480.4:c.-287+15291G=	NP_004471.4:n.-287+15291G=
NM_178155.2:c.-228+15291G=	NP_835368.1:n.-228+15291G=
NM_178156.2:c.-228+59016G=	NP_835369.1:n.-228+59016G=
NR_038167.1:n.1500+15291G=
NR_038170.1:n.583+15291G=
XM_011536613.1:c.-228+57795G=	XP_011534915.1:n.-228+57795G=
XM_017021136.1:c.-228+15291G=	XP_016876625.1:n.-228+15291G=
XM_017021137.1:c.-228+15291G=	XP_016876626.1:n.-228+15291G=
XM_017021138.1:c.-228+59016G=	XP_016876627.1:n.-228+59016G=
XM_017021139.1:c.-228+57795G=	XP_016876628.1:n.-228+57795G=
NM_001371533.1:c.-228+15291G= MANE Select	NP_001358462.1:n.-228+15291G=
NM_001371534.1:c.-228+15291G=	NP_001358463.1:n.-228+15291G=
NM_001371536.1:c.-228+15291G=	NP_001358465.1:n.-228+15291G=
NM_178155.3:c.-228+15291G=	NP_835368.1:n.-228+15291G=