Canonical Allele Identifier: CA16617217
Gene: DPYD HGNC NCBI
DPYD-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 423651
ClinVar RCV Id: RCV000485311
dbSNP Id: rs1064796552
MyVariant Identifiers: chr1:g.97771777del (hg19) chr1:g.97306221del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97306224del , CM000663.2:g.97306224del GRCh38
NC_000001.10:g.97771780del , CM000663.1:g.97771780del GRCh37
NC_000001.9:g.97544368del NCBI36
NG_008807.2:g.619839del , LRG_722:g.619839del

Transcript Alleles

HGVS Amino-acid change
ENST00000370192.8:c.2135del (DPYD) MANE Select ENSP00000359211.3:p.Pro712GlnfsTer7
ENST00000370192.7:c.2135del (DPYD) ENSP00000359211.3:p.Pro712GlnfsTer7
NM_000110.3:c.2135del , LRG_722t1:c.2135del (DPYD) NP_000101.2:p.Pro712GlnfsTer7
NR_046590.1:n.164del (DPYD-AS1)
XM_005270562.3:c.1919del (DPYD) XP_005270619.2:p.Pro640GlnfsTer7
XM_006710397.2:c.2135del (DPYD) XP_006710460.1:p.Pro712GlnfsTer7
XM_006710397.3:c.2135del (DPYD) XP_006710460.1:p.Pro712GlnfsTer7
XM_017000507.1:c.2024del (DPYD) XP_016855996.1:p.Pro675GlnfsTer7
XM_017000508.2:c.1640del (DPYD) XP_016855997.1:p.Pro547GlnfsTer7
XM_017000509.2:c.1640del (DPYD) XP_016855998.1:p.Pro547GlnfsTer7
XM_017000510.1:c.1640del (DPYD) XP_016855999.1:p.Pro547GlnfsTer7
NM_000110.4:c.2135del (DPYD) MANE Select NP_000101.2:p.Pro712GlnfsTer7
Search 100 bp 5'
Search 100 bp 3'