Canonical Allele Identifier: CA1182917406
Gene: DPYD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97549612T= , CM000663.2:g.97549612T= GRCh38
NC_000001.10:g.98015168T= , CM000663.1:g.98015168T= GRCh37
NC_000001.9:g.97787756T= NCBI36
NG_008807.2:g.376448A= , LRG_722:g.376448A=

Transcript Alleles

HGVS Amino-acid change
ENST00000370192.8:c.1472A= MANE Select ENSP00000359211.3:p.Glu491=
ENST00000370192.7:c.1472A= ENSP00000359211.3:p.Glu491=
NM_000110.3:c.1472A= , LRG_722t1:c.1472A= NP_000101.2:p.Glu491=
XM_005270562.3:c.1472A= XP_005270619.2:p.Glu491=
XM_006710397.2:c.1472A= XP_006710460.1:p.Glu491=
XM_006710397.3:c.1472A= XP_006710460.1:p.Glu491=
XM_017000507.1:c.1361A= XP_016855996.1:p.Glu454=
XM_017000508.2:c.977A= XP_016855997.1:p.Glu326=
XM_017000509.2:c.977A= XP_016855998.1:p.Glu326=
XM_017000510.1:c.977A= XP_016855999.1:p.Glu326=
NM_000110.4:c.1472A= MANE Select NP_000101.2:p.Glu491=