Canonical Allele Identifier: CA1182717182
Gene: DPYD HGNC NCBI
DPYD-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97098499G= , CM000663.2:g.97098499G= GRCh38
NC_000001.10:g.97564055G= , CM000663.1:g.97564055G= GRCh37
NC_000001.9:g.97336643G= NCBI36
NG_008807.2:g.827561C= , LRG_722:g.827561C=

Transcript Alleles

HGVS Amino-acid change
ENST00000370192.8:c.2756C= (DPYD) MANE Select ENSP00000359211.3:p.Pro919=
ENST00000370192.7:c.2756C= (DPYD) ENSP00000359211.3:p.Pro919=
NM_000110.3:c.2756C= , LRG_722t1:c.2756C= (DPYD) NP_000101.2:p.Pro919=
NR_046590.1:n.64+2513G= (DPYD-AS1)
XM_005270562.3:c.2540C= (DPYD) XP_005270619.2:p.Pro847=
XM_017000507.1:c.2645C= (DPYD) XP_016855996.1:p.Pro882=
XM_017000508.2:c.2261C= (DPYD) XP_016855997.1:p.Pro754=
XM_017000509.2:c.2261C= (DPYD) XP_016855998.1:p.Pro754=
XM_017000510.1:c.2261C= (DPYD) XP_016855999.1:p.Pro754=
NM_000110.4:c.2756C= (DPYD) MANE Select NP_000101.2:p.Pro919=