Canonical Allele Identifier: CA1182758272
Gene: DPYD HGNC NCBI
DPYD-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1658503549

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97193184dup , CM000663.2:g.97193184dup GRCh38
NC_000001.10:g.97658740dup , CM000663.1:g.97658740dup GRCh37
NC_000001.9:g.97431328dup NCBI36
NG_008807.2:g.732878dup , LRG_722:g.732878dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000370192.8:c.2509dup (DPYD) MANE Select ENSP00000359211.3:p.Leu837ProfsTer8
ENST00000370192.7:c.2509dup (DPYD) ENSP00000359211.3:p.Leu837ProfsTer8
NM_000110.3:c.2509dup , LRG_722t1:c.2509dup (DPYD) NP_000101.2:p.Leu837ProfsTer8
NR_046590.1:n.65-72230dup (DPYD-AS1)
XM_005270562.3:c.2293dup (DPYD) XP_005270619.2:p.Leu765ProfsTer8
XM_006710397.2:c.2509dup (DPYD) XP_006710460.1:p.Leu837ProfsTer8
XM_006710397.3:c.2509dup (DPYD) XP_006710460.1:p.Leu837ProfsTer8
XM_017000507.1:c.2398dup (DPYD) XP_016855996.1:p.Leu800ProfsTer8
XM_017000508.2:c.2014dup (DPYD) XP_016855997.1:p.Leu672ProfsTer8
XM_017000509.2:c.2014dup (DPYD) XP_016855998.1:p.Leu672ProfsTer8
XM_017000510.1:c.2014dup (DPYD) XP_016855999.1:p.Leu672ProfsTer8
NM_000110.4:c.2509dup (DPYD) MANE Select NP_000101.2:p.Leu837ProfsTer8