Canonical Allele Identifier: CA341374882
Gene: DPYD HGNC NCBI
DPYD-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.97564135T>A (hg19) chr1:g.97098579T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97098579T>A , CM000663.2:g.97098579T>A GRCh38
NC_000001.10:g.97564135T>A , CM000663.1:g.97564135T>A GRCh37
NC_000001.9:g.97336723T>A NCBI36
NG_008807.2:g.827481A>T , LRG_722:g.827481A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000370192.8:c.2676A>T (DPYD) MANE Select ENSP00000359211.3:p.Glu892Asp
ENST00000370192.7:c.2676A>T (DPYD) ENSP00000359211.3:p.Glu892Asp
NM_000110.3:c.2676A>T , LRG_722t1:c.2676A>T (DPYD) NP_000101.2:p.Glu892Asp
NR_046590.1:n.64+2593T>A (DPYD-AS1)
XM_005270562.3:c.2460A>T (DPYD) XP_005270619.2:p.Glu820Asp
XM_017000507.1:c.2565A>T (DPYD) XP_016855996.1:p.Glu855Asp
XM_017000508.2:c.2181A>T (DPYD) XP_016855997.1:p.Glu727Asp
XM_017000509.2:c.2181A>T (DPYD) XP_016855998.1:p.Glu727Asp
XM_017000510.1:c.2181A>T (DPYD) XP_016855999.1:p.Glu727Asp
NM_000110.4:c.2676A>T (DPYD) MANE Select NP_000101.2:p.Glu892Asp
Search 100 bp 5'
Search 100 bp 3'