Canonical Allele Identifier: CA406703107
Gene: FUT1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49254094A>T (hg19) chr19:g.48750837A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48750837A>T , CM000681.2:g.48750837A>T GRCh38
NC_000019.9:g.49254094A>T , CM000681.1:g.49254094A>T GRCh37
NC_000019.8:g.53945906A>T NCBI36
NG_007510.1:g.9554T>A
NG_007510.2:g.9554T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000645652.2:c.445T>A MANE Select ENSP00000494643.1:p.Trp149Arg
ENST00000310160.7:c.445T>A ENSP00000312021.3:p.Trp149Arg
NM_000148.3:c.445T>A NP_000139.1:p.Trp149Arg
XM_006723127.1:c.814T>A XP_006723190.1:p.Trp272Arg
NM_001329877.1:c.445T>A NP_001316806.1:p.Trp149Arg
NM_000148.4:c.445T>A NP_000139.1:p.Trp149Arg
NM_001384359.1:c.445T>A MANE Select NP_001371288.1:p.Trp149Arg
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