Canonical Allele Identifier: CA2143138323
Gene: FUT8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65471092_65471095delinsTGTG , CM000676.2:g.65471092_65471095delinsTGTG GRCh38
NC_000014.8:g.65937810_65937813delinsTGTG , CM000676.1:g.65937810_65937813delinsTGTG GRCh37
NC_000014.7:g.65007563_65007566delinsTGTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000673929.1:c.-228+15374_-228+15377delinsTGTG MANE Select ENSP00000501213.1:n.-228+15374_-228+15377delinsTGTG
ENST00000674118.1:c.-228+15374_-228+15377delinsTGTG ENSP00000501008.1:n.-228+15374_-228+15377delinsTGTG
ENST00000342677.10:c.-228+15374_-228+15377delinsTGTG ENSP00000345865.6:n.-228+15374_-228+15377delinsTGTG
ENST00000358307.6:c.-287+15374_-287+15377delinsTGTG ENSP00000351057.2:n.-287+15374_-287+15377delinsTGTG
ENST00000360689.9:c.-228+15374_-228+15377delinsTGTG ENSP00000353910.5:n.-228+15374_-228+15377delinsTGTG
ENST00000394586.6:c.-228+59099_-228+59102delinsTGTG ENSP00000378087.2:n.-228+59099_-228+59102delinsTGTG
ENST00000553924.5:c.-374+15374_-374+15377delinsTGTG ENSP00000451577.1:n.-374+15374_-374+15377delinsTGTG
ENST00000554610.1:c.-228+57878_-228+57881delinsTGTG ENSP00000452309.1:n.-228+57878_-228+57881delinsTGTG
ENST00000555559.5:c.-305-8615_-305-8612delinsTGTG ENSP00000451689.1:n.-305-8615_-305-8612delinsTGTG
ENST00000556518.5:c.-228+15374_-228+15377delinsTGTG ENSP00000452597.1:n.-228+15374_-228+15377delinsTGTG
ENST00000557164.5:c.-287+15374_-287+15377delinsTGTG ENSP00000452433.1:n.-287+15374_-287+15377delinsTGTG
ENST00000557338.5:c.-305-8615_-305-8612delinsTGTG ENSP00000452105.1:n.-305-8615_-305-8612delinsTGTG
NM_004480.4:c.-287+15374_-287+15377delinsTGTG NP_004471.4:n.-287+15374_-287+15377delinsTGTG
NM_178155.2:c.-228+15374_-228+15377delinsTGTG NP_835368.1:n.-228+15374_-228+15377delinsTGTG
NM_178156.2:c.-228+59099_-228+59102delinsTGTG NP_835369.1:n.-228+59099_-228+59102delinsTGTG
NR_038167.1:n.1500+15374_1500+15377delinsTGTG
NR_038170.1:n.583+15374_583+15377delinsTGTG
XM_011536613.1:c.-228+57878_-228+57881delinsTGTG XP_011534915.1:n.-228+57878_-228+57881delinsTGTG
XM_017021136.1:c.-228+15374_-228+15377delinsTGTG XP_016876625.1:n.-228+15374_-228+15377delinsTGTG
XM_017021137.1:c.-228+15374_-228+15377delinsTGTG XP_016876626.1:n.-228+15374_-228+15377delinsTGTG
XM_017021138.1:c.-228+59099_-228+59102delinsTGTG XP_016876627.1:n.-228+59099_-228+59102delinsTGTG
XM_017021139.1:c.-228+57878_-228+57881delinsTGTG XP_016876628.1:n.-228+57878_-228+57881delinsTGTG
NM_001371533.1:c.-228+15374_-228+15377delinsTGTG MANE Select NP_001358462.1:n.-228+15374_-228+15377delinsTGTG
NM_001371534.1:c.-228+15374_-228+15377delinsTGTG NP_001358463.1:n.-228+15374_-228+15377delinsTGTG
NM_001371536.1:c.-228+15374_-228+15377delinsTGTG NP_001358465.1:n.-228+15374_-228+15377delinsTGTG
NM_178155.3:c.-228+15374_-228+15377delinsTGTG NP_835368.1:n.-228+15374_-228+15377delinsTGTG