Canonical Allele Identifier: CA341374807
Gene: DPYD HGNC NCBI
DPYD-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1416074059
gnomAD v2: 1-97564103-G-A
gnomAD v4: 1-97098547-G-A
COSMIC: COSM3493625
MyVariant Identifiers: chr1:g.97564103G>A (hg19) chr1:g.97098547G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97098547G>A , CM000663.2:g.97098547G>A GRCh38
NC_000001.10:g.97564103G>A , CM000663.1:g.97564103G>A GRCh37
NC_000001.9:g.97336691G>A NCBI36
NG_008807.2:g.827513C>T , LRG_722:g.827513C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370192.8:c.2708C>T (DPYD) MANE Select ENSP00000359211.3:p.Ala903Val
ENST00000370192.7:c.2708C>T (DPYD) ENSP00000359211.3:p.Ala903Val
NM_000110.3:c.2708C>T , LRG_722t1:c.2708C>T (DPYD) NP_000101.2:p.Ala903Val
NR_046590.1:n.64+2561G>A (DPYD-AS1)
XM_005270562.3:c.2492C>T (DPYD) XP_005270619.2:p.Ala831Val
XM_017000507.1:c.2597C>T (DPYD) XP_016855996.1:p.Ala866Val
XM_017000508.2:c.2213C>T (DPYD) XP_016855997.1:p.Ala738Val
XM_017000509.2:c.2213C>T (DPYD) XP_016855998.1:p.Ala738Val
XM_017000510.1:c.2213C>T (DPYD) XP_016855999.1:p.Ala738Val
NM_000110.4:c.2708C>T (DPYD) MANE Select NP_000101.2:p.Ala903Val
Search 100 bp 5'
Search 100 bp 3'