Linked Data
dbSNP Id:
rs1484757629
gnomAD v3:
1-97098560-C-A
gnomAD v4:
1-97098560-C-A
COSMIC:
COSM913580
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.97098560C>A , CM000663.2:g.97098560C>A | GRCh38 |
| NC_000001.10:g.97564116C>A , CM000663.1:g.97564116C>A | GRCh37 |
| NC_000001.9:g.97336704C>A | NCBI36 |
| NG_008807.2:g.827500G>T , LRG_722:g.827500G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370192.8:c.2695G>T (DPYD) MANE Select | ENSP00000359211.3:p.Glu899Ter | |
| ENST00000370192.7:c.2695G>T (DPYD) | ENSP00000359211.3:p.Glu899Ter | |
| NM_000110.3:c.2695G>T , LRG_722t1:c.2695G>T (DPYD) | NP_000101.2:p.Glu899Ter | |
| NR_046590.1:n.64+2574C>A (DPYD-AS1) | ||
| XM_005270562.3:c.2479G>T (DPYD) | XP_005270619.2:p.Glu827Ter | |
| XM_017000507.1:c.2584G>T (DPYD) | XP_016855996.1:p.Glu862Ter | |
| XM_017000508.2:c.2200G>T (DPYD) | XP_016855997.1:p.Glu734Ter | |
| XM_017000509.2:c.2200G>T (DPYD) | XP_016855998.1:p.Glu734Ter | |
| XM_017000510.1:c.2200G>T (DPYD) | XP_016855999.1:p.Glu734Ter | |
| NM_000110.4:c.2695G>T (DPYD) MANE Select | NP_000101.2:p.Glu899Ter |