Canonical Allele Identifier: CA262723213

Gene: FUT8

Linked Data

• dbSNP Id: rs111912837
• gnomAD v2: 14-65937924-G-GTT
• gnomAD v3: 14-65471206-G-GTT
• gnomAD v4: 14-65471206-G-GTT
• MyVariant Identifiers: chr14:g.65937924_65937925insTT (hg19) ; chr14:g.65471206_65471207insTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65471207_65471208dup , CM000676.2:g.65471207_65471208dup	GRCh38
NC_000014.8:g.65937925_65937926dup , CM000676.1:g.65937925_65937926dup	GRCh37
NC_000014.7:g.65007678_65007679dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673929.1:c.-228+15489_-228+15490dup MANE Select	ENSP00000501213.1:n.-228+15489_-228+15490dup
ENST00000674118.1:c.-228+15489_-228+15490dup	ENSP00000501008.1:n.-228+15489_-228+15490dup
ENST00000342677.10:c.-228+15489_-228+15490dup	ENSP00000345865.6:n.-228+15489_-228+15490dup
ENST00000358307.6:c.-287+15489_-287+15490dup	ENSP00000351057.2:n.-287+15489_-287+15490dup
ENST00000360689.9:c.-228+15489_-228+15490dup	ENSP00000353910.5:n.-228+15489_-228+15490dup
ENST00000394586.6:c.-228+59214_-228+59215dup	ENSP00000378087.2:n.-228+59214_-228+59215dup
ENST00000553924.5:c.-374+15489_-374+15490dup	ENSP00000451577.1:n.-374+15489_-374+15490dup
ENST00000554610.1:c.-228+57993_-228+57994dup	ENSP00000452309.1:n.-228+57993_-228+57994dup
ENST00000555559.5:c.-305-8500_-305-8499dup	ENSP00000451689.1:n.-305-8500_-305-8499dup
ENST00000556518.5:c.-228+15489_-228+15490dup	ENSP00000452597.1:n.-228+15489_-228+15490dup
ENST00000557164.5:c.-287+15489_-287+15490dup	ENSP00000452433.1:n.-287+15489_-287+15490dup
ENST00000557338.5:c.-305-8500_-305-8499dup	ENSP00000452105.1:n.-305-8500_-305-8499dup
NM_004480.4:c.-287+15489_-287+15490dup	NP_004471.4:n.-287+15489_-287+15490dup
NM_178155.2:c.-228+15489_-228+15490dup	NP_835368.1:n.-228+15489_-228+15490dup
NM_178156.2:c.-228+59214_-228+59215dup	NP_835369.1:n.-228+59214_-228+59215dup
NR_038167.1:n.1500+15489_1500+15490dup
NR_038170.1:n.583+15489_583+15490dup
XM_011536613.1:c.-228+57993_-228+57994dup	XP_011534915.1:n.-228+57993_-228+57994dup
XM_017021136.1:c.-228+15489_-228+15490dup	XP_016876625.1:n.-228+15489_-228+15490dup
XM_017021137.1:c.-228+15489_-228+15490dup	XP_016876626.1:n.-228+15489_-228+15490dup
XM_017021138.1:c.-228+59214_-228+59215dup	XP_016876627.1:n.-228+59214_-228+59215dup
XM_017021139.1:c.-228+57993_-228+57994dup	XP_016876628.1:n.-228+57993_-228+57994dup
NM_001371533.1:c.-228+15489_-228+15490dup MANE Select	NP_001358462.1:n.-228+15489_-228+15490dup
NM_001371534.1:c.-228+15489_-228+15490dup	NP_001358463.1:n.-228+15489_-228+15490dup
NM_001371536.1:c.-228+15489_-228+15490dup	NP_001358465.1:n.-228+15489_-228+15490dup
NM_178155.3:c.-228+15489_-228+15490dup	NP_835368.1:n.-228+15489_-228+15490dup