Canonical Allele Identifier: CA16040798
Gene: DPYD HGNC NCBI

Linked Data

ClinVar Variation Id: 371160
ClinVar RCV Id: RCV000411454
dbSNP Id: rs1057517055
MyVariant Identifiers: chr1:g.97839172del (hg19) chr1:g.97373616del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97373618del , CM000663.2:g.97373618del GRCh38
NC_000001.10:g.97839174del , CM000663.1:g.97839174del GRCh37
NC_000001.9:g.97611762del NCBI36
NG_008807.2:g.552444del , LRG_722:g.552444del

Transcript Alleles

HGVS Amino-acid change
ENST00000370192.8:c.2003del MANE Select ENSP00000359211.3:p.Asn668IlefsTer?
ENST00000370192.7:c.2003del ENSP00000359211.3:p.Asn668IlefsTer?
NM_000110.3:c.2003del , LRG_722t1:c.2003del NP_000101.2:p.Asn668IlefsTer?
XM_005270562.3:c.1787del XP_005270619.2:p.Asn596IlefsTer?
XM_006710397.2:c.2003del XP_006710460.1:p.Asn668IlefsTer?
XR_947619.1:n.1125-1910del
XR_947620.1:n.1124+6417del
XR_947621.1:n.1125-1910del
XM_006710397.3:c.2003del XP_006710460.1:p.Asn668IlefsTer?
XM_017000507.1:c.1892del XP_016855996.1:p.Asn631IlefsTer?
XM_017000508.2:c.1508del XP_016855997.1:p.Asn503IlefsTer?
XM_017000509.2:c.1508del XP_016855998.1:p.Asn503IlefsTer?
XM_017000510.1:c.1508del XP_016855999.1:p.Asn503IlefsTer?
NM_000110.4:c.2003del MANE Select NP_000101.2:p.Asn668IlefsTer?
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