Canonical Allele Identifier: CA1182917372
Gene: DPYD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97549529G= , CM000663.2:g.97549529G= GRCh38
NC_000001.10:g.98015085G= , CM000663.1:g.98015085G= GRCh37
NC_000001.9:g.97787673G= NCBI36
NG_008807.2:g.376531C= , LRG_722:g.376531C=

Transcript Alleles

HGVS Amino-acid change
ENST00000370192.8:c.1524+31C= MANE Select ENSP00000359211.3:n.1524+31C=
ENST00000370192.7:c.1524+31C= ENSP00000359211.3:n.1524+31C=
NM_000110.3:c.1524+31C= , LRG_722t1:c.1524+31C= NP_000101.2:n.1524+31C=
XM_005270562.3:c.1524+31C= XP_005270619.2:n.1524+31C=
XM_006710397.2:c.1524+31C= XP_006710460.1:n.1524+31C=
XM_006710397.3:c.1524+31C= XP_006710460.1:n.1524+31C=
XM_017000507.1:c.1413+31C= XP_016855996.1:n.1413+31C=
XM_017000508.2:c.1029+31C= XP_016855997.1:n.1029+31C=
XM_017000509.2:c.1029+31C= XP_016855998.1:n.1029+31C=
XM_017000510.1:c.1029+31C= XP_016855999.1:n.1029+31C=
NM_000110.4:c.1524+31C= MANE Select NP_000101.2:n.1524+31C=