Canonical Allele Identifier: CA16040795
Gene: DPYD HGNC NCBI
DPYD-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 370868
ClinVar RCV Id: RCV000412243
dbSNP Id: rs1057516828
MyVariant Identifiers: chr1:g.97770827_97770828insT (hg19) chr1:g.97305271_97305272insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97305271_97305272insT , CM000663.2:g.97305271_97305272insT GRCh38
NC_000001.10:g.97770827_97770828insT , CM000663.1:g.97770827_97770828insT GRCh37
NC_000001.9:g.97543415_97543416insT NCBI36
NG_008807.2:g.620788_620789insA , LRG_722:g.620788_620789insA

Transcript Alleles

HGVS Amino-acid change
ENST00000370192.8:c.2286_2287insA (DPYD) MANE Select ENSP00000359211.3:p.Gly763ArgfsTer?
ENST00000370192.7:c.2286_2287insA (DPYD) ENSP00000359211.3:p.Gly763ArgfsTer?
NM_000110.3:c.2286_2287insA , LRG_722t1:c.2286_2287insA (DPYD) NP_000101.2:p.Gly763ArgfsTer?
NR_046590.1:n.129-918_129-917insT (DPYD-AS1)
XM_005270562.3:c.2070_2071insA (DPYD) XP_005270619.2:p.Gly691ArgfsTer?
XM_006710397.2:c.2286_2287insA (DPYD) XP_006710460.1:p.Gly763ArgfsTer?
XM_006710397.3:c.2286_2287insA (DPYD) XP_006710460.1:p.Gly763ArgfsTer?
XM_017000507.1:c.2175_2176insA (DPYD) XP_016855996.1:p.Gly726ArgfsTer?
XM_017000508.2:c.1791_1792insA (DPYD) XP_016855997.1:p.Gly598ArgfsTer?
XM_017000509.2:c.1791_1792insA (DPYD) XP_016855998.1:p.Gly598ArgfsTer?
XM_017000510.1:c.1791_1792insA (DPYD) XP_016855999.1:p.Gly598ArgfsTer?
NM_000110.4:c.2286_2287insA (DPYD) MANE Select NP_000101.2:p.Gly763ArgfsTer?
Search 100 bp 5'
Search 100 bp 3'