Canonical Allele Identifier: CA341374738
Gene: DPYD HGNC NCBI
DPYD-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.97564073A>G (hg19) chr1:g.97098517A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97098517A>G , CM000663.2:g.97098517A>G GRCh38
NC_000001.10:g.97564073A>G , CM000663.1:g.97564073A>G GRCh37
NC_000001.9:g.97336661A>G NCBI36
NG_008807.2:g.827543T>C , LRG_722:g.827543T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000370192.8:c.2738T>C (DPYD) MANE Select ENSP00000359211.3:p.Ile913Thr
ENST00000370192.7:c.2738T>C (DPYD) ENSP00000359211.3:p.Ile913Thr
NM_000110.3:c.2738T>C , LRG_722t1:c.2738T>C (DPYD) NP_000101.2:p.Ile913Thr
NR_046590.1:n.64+2531A>G (DPYD-AS1)
XM_005270562.3:c.2522T>C (DPYD) XP_005270619.2:p.Ile841Thr
XM_017000507.1:c.2627T>C (DPYD) XP_016855996.1:p.Ile876Thr
XM_017000508.2:c.2243T>C (DPYD) XP_016855997.1:p.Ile748Thr
XM_017000509.2:c.2243T>C (DPYD) XP_016855998.1:p.Ile748Thr
XM_017000510.1:c.2243T>C (DPYD) XP_016855999.1:p.Ile748Thr
NM_000110.4:c.2738T>C (DPYD) MANE Select NP_000101.2:p.Ile913Thr
Search 100 bp 5'
Search 100 bp 3'