Canonical Allele Identifier: CA2646706232
Gene: DPYD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97549621del , CM000663.2:g.97549621del GRCh38
NC_000001.10:g.98015177del , CM000663.1:g.98015177del GRCh37
NC_000001.9:g.97787765del NCBI36
NG_008807.2:g.376439del , LRG_722:g.376439del

Transcript Alleles

HGVS Amino-acid change
ENST00000370192.8:c.1463del MANE Select ENSP00000359211.3:p.Thr488IlefsTer6
ENST00000370192.7:c.1463del ENSP00000359211.3:p.Thr488IlefsTer6
NM_000110.3:c.1463del , LRG_722t1:c.1463del NP_000101.2:p.Thr488IlefsTer6
XM_005270562.3:c.1463del XP_005270619.2:p.Thr488IlefsTer6
XM_006710397.2:c.1463del XP_006710460.1:p.Thr488IlefsTer6
XM_006710397.3:c.1463del XP_006710460.1:p.Thr488IlefsTer6
XM_017000507.1:c.1352del XP_016855996.1:p.Thr451IlefsTer6
XM_017000508.2:c.968del XP_016855997.1:p.Thr323IlefsTer6
XM_017000509.2:c.968del XP_016855998.1:p.Thr323IlefsTer6
XM_017000510.1:c.968del XP_016855999.1:p.Thr323IlefsTer6
NM_000110.4:c.1463del MANE Select NP_000101.2:p.Thr488IlefsTer6