Canonical Allele Identifier: CA341373637
Gene: DPYD HGNC NCBI
DPYD-AS1 HGNC NCBI

Linked Data

gnomAD v4: 1-97193238-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97193238G>A , CM000663.2:g.97193238G>A GRCh38
NC_000001.10:g.97658794G>A , CM000663.1:g.97658794G>A GRCh37
NC_000001.9:g.97431382G>A NCBI36
NG_008807.2:g.732822C>T , LRG_722:g.732822C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370192.8:c.2453C>T (DPYD) MANE Select ENSP00000359211.3:p.Ala818Val
ENST00000370192.7:c.2453C>T (DPYD) ENSP00000359211.3:p.Ala818Val
NM_000110.3:c.2453C>T , LRG_722t1:c.2453C>T (DPYD) NP_000101.2:p.Ala818Val
NR_046590.1:n.65-72176G>A (DPYD-AS1)
XM_005270562.3:c.2237C>T (DPYD) XP_005270619.2:p.Ala746Val
XM_006710397.2:c.2453C>T (DPYD) XP_006710460.1:p.Ala818Val
XM_006710397.3:c.2453C>T (DPYD) XP_006710460.1:p.Ala818Val
XM_017000507.1:c.2342C>T (DPYD) XP_016855996.1:p.Ala781Val
XM_017000508.2:c.1958C>T (DPYD) XP_016855997.1:p.Ala653Val
XM_017000509.2:c.1958C>T (DPYD) XP_016855998.1:p.Ala653Val
XM_017000510.1:c.1958C>T (DPYD) XP_016855999.1:p.Ala653Val
NM_000110.4:c.2453C>T (DPYD) MANE Select NP_000101.2:p.Ala818Val