Canonical Allele Identifier: CA16040792
Gene: DPYD HGNC NCBI
DPYD-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 371510
ClinVar RCV Id: RCV000411332
dbSNP Id: rs1057517327
MyVariant Identifiers: chr1:g.97658658dupT (hg19) chr1:g.97658657_97658658insT (hg19) chr1:g.97193102dupT (hg38) chr1:g.97193101_97193102insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97193104dup , CM000663.2:g.97193104dup GRCh38
NC_000001.10:g.97658660dup , CM000663.1:g.97658660dup GRCh37
NC_000001.9:g.97431248dup NCBI36
NG_008807.2:g.732958dup , LRG_722:g.732958dup

Transcript Alleles

HGVS Amino-acid change
ENST00000370192.8:c.2589dup (DPYD) MANE Select ENSP00000359211.3:p.Pro864ThrfsTer7
ENST00000370192.7:c.2589dup (DPYD) ENSP00000359211.3:p.Pro864ThrfsTer7
NM_000110.3:c.2589dup , LRG_722t1:c.2589dup (DPYD) NP_000101.2:p.Pro864ThrfsTer7
NR_046590.1:n.65-72310dup (DPYD-AS1)
XM_005270562.3:c.2373dup (DPYD) XP_005270619.2:p.Pro792ThrfsTer7
XM_006710397.2:c.2589dup (DPYD) XP_006710460.1:p.Pro864ThrfsTer7
XM_006710397.3:c.2589dup (DPYD) XP_006710460.1:p.Pro864ThrfsTer7
XM_017000507.1:c.2478dup (DPYD) XP_016855996.1:p.Pro827ThrfsTer7
XM_017000508.2:c.2094dup (DPYD) XP_016855997.1:p.Pro699ThrfsTer7
XM_017000509.2:c.2094dup (DPYD) XP_016855998.1:p.Pro699ThrfsTer7
XM_017000510.1:c.2094dup (DPYD) XP_016855999.1:p.Pro699ThrfsTer7
NM_000110.4:c.2589dup (DPYD) MANE Select NP_000101.2:p.Pro864ThrfsTer7
Search 100 bp 5'
Search 100 bp 3'