Canonical Allele Identifier: CA2646704611
Gene: DPYD HGNC NCBI
DPYD-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97305296del , CM000663.2:g.97305296del GRCh38
NC_000001.10:g.97770852del , CM000663.1:g.97770852del GRCh37
NC_000001.9:g.97543440del NCBI36
NG_008807.2:g.620767del , LRG_722:g.620767del

Transcript Alleles

HGVS Amino-acid Change
ENST00000370192.8:c.2265del (DPYD) MANE Select ENSP00000359211.3:p.Ile756LeufsTer20
ENST00000370192.7:c.2265del (DPYD) ENSP00000359211.3:p.Ile756LeufsTer20
NM_000110.3:c.2265del , LRG_722t1:c.2265del (DPYD) NP_000101.2:p.Ile756LeufsTer20
NR_046590.1:n.129-893del (DPYD-AS1)
XM_005270562.3:c.2049del (DPYD) XP_005270619.2:p.Ile684LeufsTer20
XM_006710397.2:c.2265del (DPYD) XP_006710460.1:p.Ile756LeufsTer20
XM_006710397.3:c.2265del (DPYD) XP_006710460.1:p.Ile756LeufsTer20
XM_017000507.1:c.2154del (DPYD) XP_016855996.1:p.Ile719LeufsTer20
XM_017000508.2:c.1770del (DPYD) XP_016855997.1:p.Ile591LeufsTer20
XM_017000509.2:c.1770del (DPYD) XP_016855998.1:p.Ile591LeufsTer20
XM_017000510.1:c.1770del (DPYD) XP_016855999.1:p.Ile591LeufsTer20
NM_000110.4:c.2265del (DPYD) MANE Select NP_000101.2:p.Ile756LeufsTer20