Canonical Allele Identifier: CA486916728

Gene: FUT8

Linked Data

• dbSNP Id: rs1268420863
• gnomAD v3: 14-65471092-TGTG-T
• gnomAD v4: 14-65471092-TGTG-T
• MyVariant Identifiers: chr14:g.65937811_65937813del (hg19) ; chr14:g.65471093_65471095del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65471098_65471100del , CM000676.2:g.65471098_65471100del	GRCh38
NC_000014.8:g.65937816_65937818del , CM000676.1:g.65937816_65937818del	GRCh37
NC_000014.7:g.65007569_65007571del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673929.1:c.-228+15380_-228+15382del MANE Select	ENSP00000501213.1:n.-228+15380_-228+15382del
ENST00000674118.1:c.-228+15380_-228+15382del	ENSP00000501008.1:n.-228+15380_-228+15382del
ENST00000342677.10:c.-228+15380_-228+15382del	ENSP00000345865.6:n.-228+15380_-228+15382del
ENST00000358307.6:c.-287+15380_-287+15382del	ENSP00000351057.2:n.-287+15380_-287+15382del
ENST00000360689.9:c.-228+15380_-228+15382del	ENSP00000353910.5:n.-228+15380_-228+15382del
ENST00000394586.6:c.-228+59105_-228+59107del	ENSP00000378087.2:n.-228+59105_-228+59107del
ENST00000553924.5:c.-374+15380_-374+15382del	ENSP00000451577.1:n.-374+15380_-374+15382del
ENST00000554610.1:c.-228+57884_-228+57886del	ENSP00000452309.1:n.-228+57884_-228+57886del
ENST00000555559.5:c.-305-8609_-305-8607del	ENSP00000451689.1:n.-305-8609_-305-8607del
ENST00000556518.5:c.-228+15380_-228+15382del	ENSP00000452597.1:n.-228+15380_-228+15382del
ENST00000557164.5:c.-287+15380_-287+15382del	ENSP00000452433.1:n.-287+15380_-287+15382del
ENST00000557338.5:c.-305-8609_-305-8607del	ENSP00000452105.1:n.-305-8609_-305-8607del
NM_004480.4:c.-287+15380_-287+15382del	NP_004471.4:n.-287+15380_-287+15382del
NM_178155.2:c.-228+15380_-228+15382del	NP_835368.1:n.-228+15380_-228+15382del
NM_178156.2:c.-228+59105_-228+59107del	NP_835369.1:n.-228+59105_-228+59107del
NR_038167.1:n.1500+15380_1500+15382del
NR_038170.1:n.583+15380_583+15382del
XM_011536613.1:c.-228+57884_-228+57886del	XP_011534915.1:n.-228+57884_-228+57886del
XM_017021136.1:c.-228+15380_-228+15382del	XP_016876625.1:n.-228+15380_-228+15382del
XM_017021137.1:c.-228+15380_-228+15382del	XP_016876626.1:n.-228+15380_-228+15382del
XM_017021138.1:c.-228+59105_-228+59107del	XP_016876627.1:n.-228+59105_-228+59107del
XM_017021139.1:c.-228+57884_-228+57886del	XP_016876628.1:n.-228+57884_-228+57886del
NM_001371533.1:c.-228+15380_-228+15382del MANE Select	NP_001358462.1:n.-228+15380_-228+15382del
NM_001371534.1:c.-228+15380_-228+15382del	NP_001358463.1:n.-228+15380_-228+15382del
NM_001371536.1:c.-228+15380_-228+15382del	NP_001358465.1:n.-228+15380_-228+15382del
NM_178155.3:c.-228+15380_-228+15382del	NP_835368.1:n.-228+15380_-228+15382del