Canonical Allele Identifier: CA341374895
Gene: DPYD HGNC NCBI
DPYD-AS1 HGNC NCBI

Linked Data

gnomAD v4: 1-97098584-C-T
MyVariant Identifiers: chr1:g.97564140C>T (hg19) chr1:g.97098584C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97098584C>T , CM000663.2:g.97098584C>T GRCh38
NC_000001.10:g.97564140C>T , CM000663.1:g.97564140C>T GRCh37
NC_000001.9:g.97336728C>T NCBI36
NG_008807.2:g.827476G>A , LRG_722:g.827476G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370192.8:c.2671G>A (DPYD) MANE Select ENSP00000359211.3:p.Ala891Thr
ENST00000370192.7:c.2671G>A (DPYD) ENSP00000359211.3:p.Ala891Thr
NM_000110.3:c.2671G>A , LRG_722t1:c.2671G>A (DPYD) NP_000101.2:p.Ala891Thr
NR_046590.1:n.64+2598C>T (DPYD-AS1)
XM_005270562.3:c.2455G>A (DPYD) XP_005270619.2:p.Ala819Thr
XM_017000507.1:c.2560G>A (DPYD) XP_016855996.1:p.Ala854Thr
XM_017000508.2:c.2176G>A (DPYD) XP_016855997.1:p.Ala726Thr
XM_017000509.2:c.2176G>A (DPYD) XP_016855998.1:p.Ala726Thr
XM_017000510.1:c.2176G>A (DPYD) XP_016855999.1:p.Ala726Thr
NM_000110.4:c.2671G>A (DPYD) MANE Select NP_000101.2:p.Ala891Thr
Search 100 bp 5'
Search 100 bp 3'