Canonical Allele Identifier: CA658824634

Gene: FUT8

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65724328G>T , CM000676.2:g.65724328G>T	GRCh38
NC_000014.8:g.66191046G>T , CM000676.1:g.66191046G>T	GRCh37
NC_000014.7:g.65260799G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001371533.1:c.1259+5G>T MANE Select	NP_001358462.1:n.1259+5G>T
ENST00000673929.1:c.1259+5G>T MANE Select	ENSP00000501213.1:n.1259+5G>T
NM_001371534.1:c.1259+5G>T	NP_001358463.1:n.1259+5G>T
NM_001371536.1:c.1361+5G>T	NP_001358465.1:n.1361+5G>T
NM_004480.4:c.770+5G>T	NP_004471.4:n.770+5G>T
NM_178155.2:c.1259+5G>T	NP_835368.1:n.1259+5G>T
NM_178155.3:c.1259+5G>T	NP_835368.1:n.1259+5G>T
NM_178156.2:c.1259+5G>T	NP_835369.1:n.1259+5G>T
NR_038167.1:n.2563-8903G>T
NR_038170.1:n.2069+5G>T
ENST00000342677.10:c.836-8903G>T	ENSP00000345865.6:n.836-8903G>T
ENST00000358307.6:c.872+5G>T	ENSP00000351057.2:n.872+5G>T
ENST00000360689.9:c.1259+5G>T	ENSP00000353910.5:n.1259+5G>T
ENST00000394586.6:c.1259+5G>T	ENSP00000378087.2:n.1259+5G>T
ENST00000557164.5:c.770+5G>T	ENSP00000452433.1:n.770+5G>T
ENST00000674118.1:c.1259+5G>T	ENSP00000501008.1:n.1259+5G>T
XM_011536613.1:c.1259+5G>T	XP_011534915.1:n.1259+5G>T
XM_011536614.1:c.566+5G>T	XP_011534916.1:n.566+5G>T
XM_011536614.3:c.566+5G>T	XP_011534916.1:n.566+5G>T
XM_017021136.1:c.1361+5G>T	XP_016876625.1:n.1361+5G>T
XM_017021137.1:c.1361+5G>T	XP_016876626.1:n.1361+5G>T
XM_017021138.1:c.1361+5G>T	XP_016876627.1:n.1361+5G>T
XM_017021139.1:c.1361+5G>T	XP_016876628.1:n.1361+5G>T
XM_017021140.1:c.1172+5G>T	XP_016876629.1:n.1172+5G>T