Canonical Allele Identifier: CA262808190

Gene: FUT8

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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