Canonical Allele Identifier: CA390119726

Gene: FUT8

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65561575G>A , CM000676.2:g.65561575G>A	GRCh38
NC_000014.8:g.66028293G>A , CM000676.1:g.66028293G>A	GRCh37
NC_000014.7:g.65098046G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001371533.1:c.12G>A MANE Select	NP_001358462.1:p.Trp4Ter
ENST00000673929.1:c.12G>A MANE Select	ENSP00000501213.1:p.Trp4Ter
NM_001371534.1:c.12G>A	NP_001358463.1:p.Trp4Ter
NM_001371536.1:c.12G>A	NP_001358465.1:p.Trp4Ter
NM_004480.4:c.-286-54403G>A	NP_004471.4:n.-286-54403G>A
NM_178155.2:c.12G>A	NP_835368.1:p.Trp4Ter
NM_178155.3:c.12G>A	NP_835368.1:p.Trp4Ter
NM_178156.2:c.12G>A	NP_835369.1:p.Trp4Ter
NR_038167.1:n.1739G>A
NR_038170.1:n.822G>A
ENST00000342677.10:c.12G>A	ENSP00000345865.6:p.Trp4Ter
ENST00000358307.6:c.-286-54403G>A	ENSP00000351057.2:n.-286-54403G>A
ENST00000360689.9:c.12G>A	ENSP00000353910.5:p.Trp4Ter
ENST00000394586.6:c.12G>A	ENSP00000378087.2:p.Trp4Ter
ENST00000553924.5:c.12G>A	ENSP00000451577.1:p.Trp4Ter
ENST00000554610.1:c.12G>A	ENSP00000452309.1:p.Trp4Ter
ENST00000554667.1:c.12G>A	ENSP00000452147.1:p.Trp4Ter
ENST00000555559.5:c.12G>A	ENSP00000451689.1:p.Trp4Ter
ENST00000556518.5:c.12G>A	ENSP00000452597.1:p.Trp4Ter
ENST00000557164.5:c.-286-54403G>A	ENSP00000452433.1:n.-286-54403G>A
ENST00000557338.5:c.12G>A	ENSP00000452105.1:p.Trp4Ter
ENST00000674118.1:c.12G>A	ENSP00000501008.1:p.Trp4Ter
XM_011536613.1:c.12G>A	XP_011534915.1:p.Trp4Ter
XM_017021136.1:c.12G>A	XP_016876625.1:p.Trp4Ter
XM_017021137.1:c.12G>A	XP_016876626.1:p.Trp4Ter
XM_017021138.1:c.12G>A	XP_016876627.1:p.Trp4Ter
XM_017021139.1:c.12G>A	XP_016876628.1:p.Trp4Ter