Canonical Allele Identifier: CA1182979304
Gene: DPYD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97691718T= , CM000663.2:g.97691718T= GRCh38
NC_000001.10:g.98157274T= , CM000663.1:g.98157274T= GRCh37
NC_000001.9:g.97929862T= NCBI36
NG_008807.2:g.234342A= , LRG_722:g.234342A=

Transcript Alleles

HGVS Amino-acid change
ENST00000370192.8:c.761A= MANE Select ENSP00000359211.3:p.Lys254=
ENST00000370192.7:c.761A= ENSP00000359211.3:p.Lys254=
ENST00000474241.1:n.525A=
NM_000110.3:c.761A= , LRG_722t1:c.761A= NP_000101.2:p.Lys254=
XM_005270562.3:c.761A= XP_005270619.2:p.Lys254=
XM_006710397.2:c.761A= XP_006710460.1:p.Lys254=
XM_006710397.3:c.761A= XP_006710460.1:p.Lys254=
XM_017000507.1:c.650A= XP_016855996.1:p.Lys217=
XM_017000508.2:c.266A= XP_016855997.1:p.Lys89=
XM_017000509.2:c.266A= XP_016855998.1:p.Lys89=
XM_017000510.1:c.266A= XP_016855999.1:p.Lys89=
NM_000110.4:c.761A= MANE Select NP_000101.2:p.Lys254=