Canonical Allele Identifier: CA1182717186
Gene: DPYD HGNC NCBI
DPYD-AS1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000370192.8:c.2749C= (DPYD) MANE Select ENSP00000359211.3:p.Pro917=
ENST00000370192.7:c.2749C= (DPYD) ENSP00000359211.3:p.Pro917=
NM_000110.3:c.2749C= , LRG_722t1:c.2749C= (DPYD) NP_000101.2:p.Pro917=
NR_046590.1:n.64+2520G= (DPYD-AS1)
XM_005270562.3:c.2533C= (DPYD) XP_005270619.2:p.Pro845=
XM_017000507.1:c.2638C= (DPYD) XP_016855996.1:p.Pro880=
XM_017000508.2:c.2254C= (DPYD) XP_016855997.1:p.Pro752=
XM_017000509.2:c.2254C= (DPYD) XP_016855998.1:p.Pro752=
XM_017000510.1:c.2254C= (DPYD) XP_016855999.1:p.Pro752=
NM_000110.4:c.2749C= (DPYD) MANE Select NP_000101.2:p.Pro917=