Canonical Allele Identifier: CA2340030209
Gene: FUT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48703733_48703736delinsTGTG , CM000681.2:g.48703733_48703736delinsTGTG GRCh38
NC_000019.9:g.49206990_49206993delinsTGTG , CM000681.1:g.49206990_49206993delinsTGTG GRCh37
NC_000019.8:g.53898802_53898805delinsTGTG NCBI36
NG_007511.1:g.12763_12766delinsTGTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000425340.3:c.777_780delinsTGTG MANE Select ENSP00000387498.2:p.Asp259=
ENST00000522966.2:c.777_780delinsTGTG ENSP00000430227.2:p.Asp259=
ENST00000391876.5:c.777_780delinsTGTG ENSP00000375748.4:p.Asp259=
ENST00000425340.2:c.777_780delinsTGTG ENSP00000387498.2:p.Asp259=
NM_000511.5:c.777_780delinsTGTG NP_000502.4:p.Asp259=
NM_001097638.2:c.777_780delinsTGTG NP_001091107.1:p.Asp259=
NR_131188.1:n.113_116delinsCACA
NM_000511.6:c.777_780delinsTGTG MANE Select NP_000502.4:p.Asp259=
NM_001097638.3:c.777_780delinsTGTG NP_001091107.1:p.Asp259=