Canonical Allele Identifier: CA2646706807
Gene: DPYD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97691229del , CM000663.2:g.97691229del GRCh38
NC_000001.10:g.98156785del , CM000663.1:g.98156785del GRCh37
NC_000001.9:g.97929373del NCBI36
NG_008807.2:g.234836del , LRG_722:g.234836del

Transcript Alleles

HGVS Amino-acid Change
ENST00000370192.8:c.762+493del MANE Select ENSP00000359211.3:n.762+493del
ENST00000370192.7:c.762+493del ENSP00000359211.3:n.762+493del
ENST00000474241.1:n.1019del
NM_000110.3:c.762+493del , LRG_722t1:c.762+493del NP_000101.2:n.762+493del
XM_005270562.3:c.762+493del XP_005270619.2:n.762+493del
XM_006710397.2:c.762+493del XP_006710460.1:n.762+493del
XM_006710397.3:c.762+493del XP_006710460.1:n.762+493del
XM_017000507.1:c.651+493del XP_016855996.1:n.651+493del
XM_017000508.2:c.267+493del XP_016855997.1:n.267+493del
XM_017000509.2:c.267+493del XP_016855998.1:n.267+493del
XM_017000510.1:c.267+493del XP_016855999.1:n.267+493del
NM_000110.4:c.762+493del MANE Select NP_000101.2:n.762+493del