Canonical Allele Identifier: CA7233315

Gene: FUT8

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65669445C>A , CM000676.2:g.65669445C>A	GRCh38
NC_000014.8:g.66136163C>A , CM000676.1:g.66136163C>A	GRCh37
NC_000014.7:g.65205916C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001371533.1:c.800C>A MANE Select	NP_001358462.1:p.Thr267Lys
ENST00000673929.1:c.800C>A MANE Select	ENSP00000501213.1:p.Thr267Lys
NM_001371534.1:c.800C>A	NP_001358463.1:p.Thr267Lys
NM_001371536.1:c.902C>A	NP_001358465.1:p.Thr301Lys
NM_004480.4:c.311C>A	NP_004471.4:p.Thr104Lys
NM_178155.2:c.800C>A	NP_835368.1:p.Thr267Lys
NM_178155.3:c.800C>A	NP_835368.1:p.Thr267Lys
NM_178156.2:c.800C>A	NP_835369.1:p.Thr267Lys
NR_038167.1:n.2527C>A
NR_038170.1:n.1610C>A
ENST00000342677.10:c.800C>A	ENSP00000345865.6:p.Thr267Lys
ENST00000358307.6:c.413C>A	ENSP00000351057.2:p.Thr138Lys
ENST00000360689.9:c.800C>A	ENSP00000353910.5:p.Thr267Lys
ENST00000394586.6:c.800C>A	ENSP00000378087.2:p.Thr267Lys
ENST00000554765.1:n.546C>A
ENST00000557164.5:c.311C>A	ENSP00000452433.1:p.Thr104Lys
ENST00000557536.5:n.389C>A
ENST00000674118.1:c.800C>A	ENSP00000501008.1:p.Thr267Lys
XM_011536613.1:c.800C>A	XP_011534915.1:p.Thr267Lys
XM_011536614.1:c.107C>A	XP_011534916.1:p.Thr36Lys
XM_011536614.3:c.107C>A	XP_011534916.1:p.Thr36Lys
XM_017021136.1:c.902C>A	XP_016876625.1:p.Thr301Lys
XM_017021137.1:c.902C>A	XP_016876626.1:p.Thr301Lys
XM_017021138.1:c.902C>A	XP_016876627.1:p.Thr301Lys
XM_017021139.1:c.902C>A	XP_016876628.1:p.Thr301Lys
XM_017021140.1:c.713C>A	XP_016876629.1:p.Thr238Lys