Canonical Allele Identifier: CA341374713
Gene: DPYD HGNC NCBI
DPYD-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97098506G>T , CM000663.2:g.97098506G>T GRCh38
NC_000001.10:g.97564062G>T , CM000663.1:g.97564062G>T GRCh37
NC_000001.9:g.97336650G>T NCBI36
NG_008807.2:g.827554C>A , LRG_722:g.827554C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000370192.8:c.2749C>A (DPYD) MANE Select ENSP00000359211.3:p.Pro917Thr
ENST00000370192.7:c.2749C>A (DPYD) ENSP00000359211.3:p.Pro917Thr
NM_000110.3:c.2749C>A , LRG_722t1:c.2749C>A (DPYD) NP_000101.2:p.Pro917Thr
NR_046590.1:n.64+2520G>T (DPYD-AS1)
XM_005270562.3:c.2533C>A (DPYD) XP_005270619.2:p.Pro845Thr
XM_017000507.1:c.2638C>A (DPYD) XP_016855996.1:p.Pro880Thr
XM_017000508.2:c.2254C>A (DPYD) XP_016855997.1:p.Pro752Thr
XM_017000509.2:c.2254C>A (DPYD) XP_016855998.1:p.Pro752Thr
XM_017000510.1:c.2254C>A (DPYD) XP_016855999.1:p.Pro752Thr
NM_000110.4:c.2749C>A (DPYD) MANE Select NP_000101.2:p.Pro917Thr