Canonical Allele Identifier: CA16040788
Gene: DPYD HGNC NCBI
DPYD-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 370956
ClinVar RCV Id: RCV000412342
dbSNP Id: rs1057516894
MyVariant Identifiers: chr1:g.97564057del (hg19) chr1:g.97098501del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97098502del , CM000663.2:g.97098502del GRCh38
NC_000001.10:g.97564058del , CM000663.1:g.97564058del GRCh37
NC_000001.9:g.97336646del NCBI36
NG_008807.2:g.827559del , LRG_722:g.827559del

Transcript Alleles

HGVS Amino-acid change
ENST00000370192.8:c.2754del (DPYD) MANE Select ENSP00000359211.3:p.Pro919LeufsTer6
ENST00000370192.7:c.2754del (DPYD) ENSP00000359211.3:p.Pro919LeufsTer6
NM_000110.3:c.2754del , LRG_722t1:c.2754del (DPYD) NP_000101.2:p.Pro919LeufsTer6
NR_046590.1:n.64+2516del (DPYD-AS1)
XM_005270562.3:c.2538del (DPYD) XP_005270619.2:p.Pro847LeufsTer6
XM_017000507.1:c.2643del (DPYD) XP_016855996.1:p.Pro882LeufsTer6
XM_017000508.2:c.2259del (DPYD) XP_016855997.1:p.Pro754LeufsTer6
XM_017000509.2:c.2259del (DPYD) XP_016855998.1:p.Pro754LeufsTer6
XM_017000510.1:c.2259del (DPYD) XP_016855999.1:p.Pro754LeufsTer6
NM_000110.4:c.2754del (DPYD) MANE Select NP_000101.2:p.Pro919LeufsTer6
Search 100 bp 5'
Search 100 bp 3'