Canonical Allele Identifier: CA2646706295
Gene: DPYD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97549882del , CM000663.2:g.97549882del GRCh38
NC_000001.10:g.98015438del , CM000663.1:g.98015438del GRCh37
NC_000001.9:g.97788026del NCBI36
NG_008807.2:g.376182del , LRG_722:g.376182del

Transcript Alleles

HGVS Amino-acid Change
ENST00000370192.8:c.1340-134del MANE Select ENSP00000359211.3:n.1340-134del
ENST00000370192.7:c.1340-134del ENSP00000359211.3:n.1340-134del
NM_000110.3:c.1340-134del , LRG_722t1:c.1340-134del NP_000101.2:n.1340-134del
XM_005270562.3:c.1340-134del XP_005270619.2:n.1340-134del
XM_006710397.2:c.1340-134del XP_006710460.1:n.1340-134del
XM_006710397.3:c.1340-134del XP_006710460.1:n.1340-134del
XM_017000507.1:c.1229-134del XP_016855996.1:n.1229-134del
XM_017000508.2:c.845-134del XP_016855997.1:n.845-134del
XM_017000509.2:c.845-134del XP_016855998.1:n.845-134del
XM_017000510.1:c.845-134del XP_016855999.1:n.845-134del
NM_000110.4:c.1340-134del MANE Select NP_000101.2:n.1340-134del