Canonical Allele Identifier: CA341374806
Gene: DPYD HGNC NCBI
DPYD-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.97564101A>C (hg19) chr1:g.97098545A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97098545A>C , CM000663.2:g.97098545A>C GRCh38
NC_000001.10:g.97564101A>C , CM000663.1:g.97564101A>C GRCh37
NC_000001.9:g.97336689A>C NCBI36
NG_008807.2:g.827515T>G , LRG_722:g.827515T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370192.8:c.2710T>G (DPYD) MANE Select ENSP00000359211.3:p.Phe904Val
ENST00000370192.7:c.2710T>G (DPYD) ENSP00000359211.3:p.Phe904Val
NM_000110.3:c.2710T>G , LRG_722t1:c.2710T>G (DPYD) NP_000101.2:p.Phe904Val
NR_046590.1:n.64+2559A>C (DPYD-AS1)
XM_005270562.3:c.2494T>G (DPYD) XP_005270619.2:p.Phe832Val
XM_017000507.1:c.2599T>G (DPYD) XP_016855996.1:p.Phe867Val
XM_017000508.2:c.2215T>G (DPYD) XP_016855997.1:p.Phe739Val
XM_017000509.2:c.2215T>G (DPYD) XP_016855998.1:p.Phe739Val
XM_017000510.1:c.2215T>G (DPYD) XP_016855999.1:p.Phe739Val
NM_000110.4:c.2710T>G (DPYD) MANE Select NP_000101.2:p.Phe904Val
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