Canonical Allele Identifier: CA2646704613
Gene: DPYD HGNC NCBI
DPYD-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97305376del , CM000663.2:g.97305376del GRCh38
NC_000001.10:g.97770932del , CM000663.1:g.97770932del GRCh37
NC_000001.9:g.97543520del NCBI36
NG_008807.2:g.620685del , LRG_722:g.620685del

Transcript Alleles

HGVS Amino-acid change
ENST00000370192.8:c.2183del (DPYD) MANE Select ENSP00000359211.3:p.Gly728ValfsTer14
ENST00000370192.7:c.2183del (DPYD) ENSP00000359211.3:p.Gly728ValfsTer14
NM_000110.3:c.2183del , LRG_722t1:c.2183del (DPYD) NP_000101.2:p.Gly728ValfsTer14
NR_046590.1:n.129-813del (DPYD-AS1)
XM_005270562.3:c.1967del (DPYD) XP_005270619.2:p.Gly656ValfsTer14
XM_006710397.2:c.2183del (DPYD) XP_006710460.1:p.Gly728ValfsTer14
XM_006710397.3:c.2183del (DPYD) XP_006710460.1:p.Gly728ValfsTer14
XM_017000507.1:c.2072del (DPYD) XP_016855996.1:p.Gly691ValfsTer14
XM_017000508.2:c.1688del (DPYD) XP_016855997.1:p.Gly563ValfsTer14
XM_017000509.2:c.1688del (DPYD) XP_016855998.1:p.Gly563ValfsTer14
XM_017000510.1:c.1688del (DPYD) XP_016855999.1:p.Gly563ValfsTer14
NM_000110.4:c.2183del (DPYD) MANE Select NP_000101.2:p.Gly728ValfsTer14