Canonical Allele Identifier: CA1148236480
Gene: DPYD HGNC NCBI
DPYD-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97098664_97098668delinsGTTAG , CM000663.2:g.97098664_97098668delinsGTTAG GRCh38
NC_000001.10:g.97564220_97564224delinsGTTAG , CM000663.1:g.97564220_97564224delinsGTTAG GRCh37
NC_000001.9:g.97336808_97336812delinsGTTAG NCBI36
NG_008807.2:g.827392_827396delinsCTAAC , LRG_722:g.827392_827396delinsCTAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000370192.8:c.2623-36_2623-32delinsCTAAC (DPYD) MANE Select ENSP00000359211.3:n.2623-36_2623-32delinsCTAAC
ENST00000370192.7:c.2623-36_2623-32delinsCTAAC (DPYD) ENSP00000359211.3:n.2623-36_2623-32delinsCTAAC
NM_000110.3:c.2623-36_2623-32delinsCTAAC , LRG_722t1:c.2623-36_2623-32delinsCTAAC (DPYD) NP_000101.2:n.2623-36_2623-32delinsCTAAC
NR_046590.1:n.64+2678_64+2682delinsGTTAG (DPYD-AS1)
XM_005270562.3:c.2407-36_2407-32delinsCTAAC (DPYD) XP_005270619.2:n.2407-36_2407-32delinsCTAAC
XM_017000507.1:c.2512-36_2512-32delinsCTAAC (DPYD) XP_016855996.1:n.2512-36_2512-32delinsCTAAC
XM_017000508.2:c.2128-36_2128-32delinsCTAAC (DPYD) XP_016855997.1:n.2128-36_2128-32delinsCTAAC
XM_017000509.2:c.2128-36_2128-32delinsCTAAC (DPYD) XP_016855998.1:n.2128-36_2128-32delinsCTAAC
XM_017000510.1:c.2128-36_2128-32delinsCTAAC (DPYD) XP_016855999.1:n.2128-36_2128-32delinsCTAAC
NM_000110.4:c.2623-36_2623-32delinsCTAAC (DPYD) MANE Select NP_000101.2:n.2623-36_2623-32delinsCTAAC