Canonical Allele Identifier: CA341374562
Gene: DPYD HGNC NCBI
DPYD-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97234941G>C , CM000663.2:g.97234941G>C GRCh38
NC_000001.10:g.97700497G>C , CM000663.1:g.97700497G>C GRCh37
NC_000001.9:g.97473085G>C NCBI36
NG_008807.2:g.691119C>G , LRG_722:g.691119C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370192.8:c.2353C>G (DPYD) MANE Select ENSP00000359211.3:p.Leu785Val
ENST00000370192.7:c.2353C>G (DPYD) ENSP00000359211.3:p.Leu785Val
NM_000110.3:c.2353C>G , LRG_722t1:c.2353C>G (DPYD) NP_000101.2:p.Leu785Val
NR_046590.1:n.65-30473G>C (DPYD-AS1)
XM_005270562.3:c.2137C>G (DPYD) XP_005270619.2:p.Leu713Val
XM_006710397.2:c.2353C>G (DPYD) XP_006710460.1:p.Leu785Val
XM_006710397.3:c.2353C>G (DPYD) XP_006710460.1:p.Leu785Val
XM_017000507.1:c.2242C>G (DPYD) XP_016855996.1:p.Leu748Val
XM_017000508.2:c.1858C>G (DPYD) XP_016855997.1:p.Leu620Val
XM_017000509.2:c.1858C>G (DPYD) XP_016855998.1:p.Leu620Val
XM_017000510.1:c.1858C>G (DPYD) XP_016855999.1:p.Leu620Val
NM_000110.4:c.2353C>G (DPYD) MANE Select NP_000101.2:p.Leu785Val