Linked Data
dbSNP Id:
rs1416074059
gnomAD v2:
1-97564103-G-A
gnomAD v4:
1-97098547-G-A
COSMIC:
COSM3493625
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 |