Canonical Allele Identifier: CA2962839713
Gene: FUT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48703566del , CM000681.2:g.48703566del GRCh38
NC_000019.9:g.49206823del , CM000681.1:g.49206823del GRCh37
NC_000019.8:g.53898635del NCBI36
NG_007511.1:g.12596del

Transcript Alleles

HGVS Amino-acid Change
ENST00000425340.3:c.610del MANE Select ENSP00000387498.2:p.Asp204ThrfsTer?
ENST00000522966.2:c.610del ENSP00000430227.2:p.Asp204ThrfsTer?
ENST00000391876.5:c.610del ENSP00000375748.4:p.Asp204ThrfsTer?
ENST00000425340.2:c.610del ENSP00000387498.2:p.Asp204ThrfsTer?
ENST00000522966.1:c.610del ENSP00000430227.1:p.Asp204ThrfsTer?
NM_000511.5:c.610del NP_000502.4:p.Asp204ThrfsTer?
NM_001097638.2:c.610del NP_001091107.1:p.Asp204ThrfsTer?
NR_131188.1:n.286del
NM_000511.6:c.610del MANE Select NP_000502.4:p.Asp204ThrfsTer?
NM_001097638.3:c.610del NP_001091107.1:p.Asp204ThrfsTer?