Canonical Allele Identifier: CA10610856
Gene: DPYD HGNC NCBI
DPYD-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 298281
ClinVar RCV Id: RCV000299078
dbSNP Id: rs762911226
MyVariant Identifiers: chr1:g.97564179T>C (hg19) chr1:g.97098623T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97098623T>C , CM000663.2:g.97098623T>C GRCh38
NC_000001.10:g.97564179T>C , CM000663.1:g.97564179T>C GRCh37
NC_000001.9:g.97336767T>C NCBI36
NG_008807.2:g.827437A>G , LRG_722:g.827437A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370192.8:c.2632A>G (DPYD) MANE Select ENSP00000359211.3:p.Ser878Gly
ENST00000370192.7:c.2632A>G (DPYD) ENSP00000359211.3:p.Ser878Gly
NM_000110.3:c.2632A>G , LRG_722t1:c.2632A>G (DPYD) NP_000101.2:p.Ser878Gly
NR_046590.1:n.64+2637T>C (DPYD-AS1)
XM_005270562.3:c.2416A>G (DPYD) XP_005270619.2:p.Ser806Gly
XM_017000507.1:c.2521A>G (DPYD) XP_016855996.1:p.Ser841Gly
XM_017000508.2:c.2137A>G (DPYD) XP_016855997.1:p.Ser713Gly
XM_017000509.2:c.2137A>G (DPYD) XP_016855998.1:p.Ser713Gly
XM_017000510.1:c.2137A>G (DPYD) XP_016855999.1:p.Ser713Gly
NM_000110.4:c.2632A>G (DPYD) MANE Select NP_000101.2:p.Ser878Gly
Search 100 bp 5'
Search 100 bp 3'