Canonical Allele Identifier: CA27484628
Gene: DPYD HGNC NCBI
DPYD-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs980732943
gnomAD v2: 1-97770823-C-T
gnomAD v3: 1-97305267-C-T
gnomAD v4: 1-97305267-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97305267C>T , CM000663.2:g.97305267C>T GRCh38
NC_000001.10:g.97770823C>T , CM000663.1:g.97770823C>T GRCh37
NC_000001.9:g.97543411C>T NCBI36
NG_008807.2:g.620793G>A , LRG_722:g.620793G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000370192.8:c.2291G>A (DPYD) MANE Select ENSP00000359211.3:p.Gly764Glu
ENST00000370192.7:c.2291G>A (DPYD) ENSP00000359211.3:p.Gly764Glu
NM_000110.3:c.2291G>A , LRG_722t1:c.2291G>A (DPYD) NP_000101.2:p.Gly764Glu
NR_046590.1:n.129-922C>T (DPYD-AS1)
XM_005270562.3:c.2075G>A (DPYD) XP_005270619.2:p.Gly692Glu
XM_006710397.2:c.2291G>A (DPYD) XP_006710460.1:p.Gly764Glu
XM_006710397.3:c.2291G>A (DPYD) XP_006710460.1:p.Gly764Glu
XM_017000507.1:c.2180G>A (DPYD) XP_016855996.1:p.Gly727Glu
XM_017000508.2:c.1796G>A (DPYD) XP_016855997.1:p.Gly599Glu
XM_017000509.2:c.1796G>A (DPYD) XP_016855998.1:p.Gly599Glu
XM_017000510.1:c.1796G>A (DPYD) XP_016855999.1:p.Gly599Glu
NM_000110.4:c.2291G>A (DPYD) MANE Select NP_000101.2:p.Gly764Glu