Canonical Allele Identifier: CA16040790
Gene: DPYD HGNC NCBI
DPYD-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 370928
ClinVar RCV Id: RCV000409198
dbSNP Id: rs1057516873

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97098575T>A , CM000663.2:g.97098575T>A GRCh38
NC_000001.10:g.97564131T>A , CM000663.1:g.97564131T>A GRCh37
NC_000001.9:g.97336719T>A NCBI36
NG_008807.2:g.827485A>T , LRG_722:g.827485A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000370192.8:c.2680A>T (DPYD) MANE Select ENSP00000359211.3:p.Lys894Ter
ENST00000370192.7:c.2680A>T (DPYD) ENSP00000359211.3:p.Lys894Ter
NM_000110.3:c.2680A>T , LRG_722t1:c.2680A>T (DPYD) NP_000101.2:p.Lys894Ter
NR_046590.1:n.64+2589T>A (DPYD-AS1)
XM_005270562.3:c.2464A>T (DPYD) XP_005270619.2:p.Lys822Ter
XM_017000507.1:c.2569A>T (DPYD) XP_016855996.1:p.Lys857Ter
XM_017000508.2:c.2185A>T (DPYD) XP_016855997.1:p.Lys729Ter
XM_017000509.2:c.2185A>T (DPYD) XP_016855998.1:p.Lys729Ter
XM_017000510.1:c.2185A>T (DPYD) XP_016855999.1:p.Lys729Ter
NM_000110.4:c.2680A>T (DPYD) MANE Select NP_000101.2:p.Lys894Ter