Canonical Allele Identifier: CA16040810
Gene: DPYD HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 370713
ClinVar RCV Id: RCV000411932
dbSNP Id: rs1057516711

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97595110del , CM000663.2:g.97595110del GRCh38
NC_000001.10:g.98060666del , CM000663.1:g.98060666del GRCh37
NC_000001.9:g.97833254del NCBI36
NG_008807.2:g.330953del , LRG_722:g.330953del

Transcript Alleles

HGVS Amino-acid change
NM_000110.3:c.910del , LRG_722t1:c.910del NP_000101.2:p.Tyr304IlefsTer10
XM_005270562.3:c.910del XP_005270619.2:p.Tyr304IlefsTer10
XM_006710397.2:c.910del XP_006710460.1:p.Tyr304IlefsTer10
XM_006710397.3:c.910del
XM_017000507.1:c.799del XP_016855996.1:p.Tyr267IlefsTer10
XM_017000508.2:c.415del XP_016855997.1:p.Tyr139IlefsTer10
XM_017000509.2:c.415del XP_016855998.1:p.Tyr139IlefsTer10
XM_017000510.1:c.415del XP_016855999.1:p.Tyr139IlefsTer10
ENST00000370192.7:c.910del ENSP00000359211.3:p.Tyr304IlefsTer10