Canonical Allele Identifier: CA2741636655
Gene: FUT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48703425_48703426insCTTTAGTGAACACATTTTTAGGCAATTATAAGAAGCTGATTA , CM000681.2:g.48703425_48703426insCTTTAGTGAACACATTTTTAGGCAATTATAAGAAGCTGATTA GRCh38
NC_000019.9:g.49206682_49206683insCTTTAGTGAACACATTTTTAGGCAATTATAAGAAGCTGATTA , CM000681.1:g.49206682_49206683insCTTTAGTGAACACATTTTTAGGCAATTATAAGAAGCTGATTA GRCh37
NC_000019.8:g.53898494_53898495insCTTTAGTGAACACATTTTTAGGCAATTATAAGAAGCTGATTA NCBI36
NG_007511.1:g.12455_12456insCTTTAGTGAACACATTTTTAGGCAATTATAAGAAGCTGATTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000425340.3:c.469_470insCTTTAGTGAACACATTTTTAGGCAATTATAAGAAGCTGATTA MANE Select ENSP00000387498.2:p.Tyr157delinsSerLeuValAsnThrPheLeuGlyAsnTy...
ENST00000522966.2:c.469_470insCTTTAGTGAACACATTTTTAGGCAATTATAAGAAGCTGATTA ENSP00000430227.2:p.Tyr157delinsSerLeuValAsnThrPheLeuGlyAsnTy...
ENST00000391876.5:c.469_470insCTTTAGTGAACACATTTTTAGGCAATTATAAGAAGCTGATTA ENSP00000375748.4:p.Tyr157delinsSerLeuValAsnThrPheLeuGlyAsnTy...
ENST00000425340.2:c.469_470insCTTTAGTGAACACATTTTTAGGCAATTATAAGAAGCTGATTA ENSP00000387498.2:p.Tyr157delinsSerLeuValAsnThrPheLeuGlyAsnTy...
ENST00000522966.1:c.469_470insCTTTAGTGAACACATTTTTAGGCAATTATAAGAAGCTGATTA ENSP00000430227.1:p.Tyr157delinsSerLeuValAsnThrPheLeuGlyAsnTy...
NM_000511.5:c.469_470insCTTTAGTGAACACATTTTTAGGCAATTATAAGAAGCTGATTA NP_000502.4:p.Tyr157delinsSerLeuValAsnThrPheLeuGlyAsnTyrLysLy...
NM_001097638.2:c.469_470insCTTTAGTGAACACATTTTTAGGCAATTATAAGAAGCTGATTA NP_001091107.1:p.Tyr157delinsSerLeuValAsnThrPheLeuGlyAsnTyrLy...
NR_131188.1:n.423_424insTAATCAGCTTCTTATAATTGCCTAAAAATGTGTTCACTAAAG
NM_000511.6:c.469_470insCTTTAGTGAACACATTTTTAGGCAATTATAAGAAGCTGATTA MANE Select NP_000502.4:p.Tyr157delinsSerLeuValAsnThrPheLeuGlyAsnTyrLysLy...
NM_001097638.3:c.469_470insCTTTAGTGAACACATTTTTAGGCAATTATAAGAAGCTGATTA NP_001091107.1:p.Tyr157delinsSerLeuValAsnThrPheLeuGlyAsnTyrLy...