Canonical Allele Identifier: CA2506093848
Gene: FUT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48703442_48703443insCC , CM000681.2:g.48703442_48703443insCC GRCh38
NC_000019.9:g.49206699_49206700insCC , CM000681.1:g.49206699_49206700insCC GRCh37
NC_000019.8:g.53898511_53898512insCC NCBI36
NG_007511.1:g.12472_12473insCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000425340.3:c.486_487insCC MANE Select ENSP00000387498.2:p.Glu163ProfsTer26
ENST00000522966.2:c.486_487insCC ENSP00000430227.2:p.Glu163ProfsTer26
ENST00000391876.5:c.486_487insCC ENSP00000375748.4:p.Glu163ProfsTer26
ENST00000425340.2:c.486_487insCC ENSP00000387498.2:p.Glu163ProfsTer26
ENST00000522966.1:c.486_487insCC ENSP00000430227.1:p.Glu163ProfsTer26
NM_000511.5:c.486_487insCC NP_000502.4:p.Glu163ProfsTer26
NM_001097638.2:c.486_487insCC NP_001091107.1:p.Glu163ProfsTer26
NR_131188.1:n.406_407insGG
NM_000511.6:c.486_487insCC MANE Select NP_000502.4:p.Glu163ProfsTer26
NM_001097638.3:c.486_487insCC NP_001091107.1:p.Glu163ProfsTer26