Canonical Allele Identifier: CA2814663949
Gene: FUT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48703719_48703720insATG , CM000681.2:g.48703719_48703720insATG GRCh38
NC_000019.9:g.49206976_49206977insATG , CM000681.1:g.49206976_49206977insATG GRCh37
NC_000019.8:g.53898788_53898789insATG NCBI36
NG_007511.1:g.12749_12750insATG

Transcript Alleles

HGVS Amino-acid Change
ENST00000425340.3:c.763_764insATG MANE Select ENSP00000387498.2:p.Thr255delinsAsnAla
ENST00000522966.2:c.763_764insATG ENSP00000430227.2:p.Thr255delinsAsnAla
ENST00000391876.5:c.763_764insATG ENSP00000375748.4:p.Thr255delinsAsnAla
ENST00000425340.2:c.763_764insATG ENSP00000387498.2:p.Thr255delinsAsnAla
NM_000511.5:c.763_764insATG NP_000502.4:p.Thr255delinsAsnAla
NM_001097638.2:c.763_764insATG NP_001091107.1:p.Thr255delinsAsnAla
NR_131188.1:n.129_130insCAT
NM_000511.6:c.763_764insATG MANE Select NP_000502.4:p.Thr255delinsAsnAla
NM_001097638.3:c.763_764insATG NP_001091107.1:p.Thr255delinsAsnAla