Canonical Allele Identifier: CA508043157
Gene: FUT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49207154del (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48703900del , CM000681.2:g.48703900del GRCh38
NC_000019.9:g.49207157del , CM000681.1:g.49207157del GRCh37
NC_000019.8:g.53898969del NCBI36
NG_007511.1:g.12930del

Transcript Alleles

HGVS Amino-acid Change
ENST00000425340.3:c.944del MANE Select ENSP00000387498.2:p.Pro315LeufsTer?
ENST00000522966.2:c.944del ENSP00000430227.2:p.Pro315LeufsTer?
ENST00000391876.5:c.944del ENSP00000375748.4:p.Pro315LeufsTer?
ENST00000425340.2:c.944del ENSP00000387498.2:p.Pro315LeufsTer?
NM_000511.5:c.944del NP_000502.4:p.Pro315LeufsTer?
NM_001097638.2:c.944del NP_001091107.1:p.Pro315LeufsTer?
NM_000511.6:c.944del MANE Select NP_000502.4:p.Pro315LeufsTer?
NM_001097638.3:c.944del NP_001091107.1:p.Pro315LeufsTer?
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