Canonical Allele Identifier: CA2838856438
Gene: FUT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48703491_48703492insCGC , CM000681.2:g.48703491_48703492insCGC GRCh38
NC_000019.9:g.49206748_49206749insCGC , CM000681.1:g.49206748_49206749insCGC GRCh37
NC_000019.8:g.53898560_53898561insCGC NCBI36
NG_007511.1:g.12521_12522insCGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000425340.3:c.535_536insCGC MANE Select ENSP00000387498.2:p.Ala178_Gln179insPro
ENST00000522966.2:c.535_536insCGC ENSP00000430227.2:p.Ala178_Gln179insPro
ENST00000391876.5:c.535_536insCGC ENSP00000375748.4:p.Ala178_Gln179insPro
ENST00000425340.2:c.535_536insCGC ENSP00000387498.2:p.Ala178_Gln179insPro
ENST00000522966.1:c.535_536insCGC ENSP00000430227.1:p.Ala178_Gln179insPro
NM_000511.5:c.535_536insCGC NP_000502.4:p.Ala178_Gln179insPro
NM_001097638.2:c.535_536insCGC NP_001091107.1:p.Ala178_Gln179insPro
NR_131188.1:n.358_359insCGG
NM_000511.6:c.535_536insCGC MANE Select NP_000502.4:p.Ala178_Gln179insPro
NM_001097638.3:c.535_536insCGC NP_001091107.1:p.Ala178_Gln179insPro