Canonical Allele Identifier: CA1182717262
Gene: DPYD HGNC NCBI
DPYD-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1650446851
gnomAD v3: 1-97098721-CAAAT-C
gnomAD v4: 1-97098721-CAAAT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97098722_97098725del , CM000663.2:g.97098722_97098725del GRCh38
NC_000001.10:g.97564278_97564281del , CM000663.1:g.97564278_97564281del GRCh37
NC_000001.9:g.97336866_97336869del NCBI36
NG_008807.2:g.827335_827338del , LRG_722:g.827335_827338del

Transcript Alleles

HGVS Amino-acid Change
ENST00000370192.8:c.2623-93_2623-90del (DPYD) MANE Select ENSP00000359211.3:n.2623-93_2623-90del
ENST00000370192.7:c.2623-93_2623-90del (DPYD) ENSP00000359211.3:n.2623-93_2623-90del
NM_000110.3:c.2623-93_2623-90del , LRG_722t1:c.2623-93_2623-90del (DPYD) NP_000101.2:n.2623-93_2623-90del
NR_046590.1:n.64+2736_64+2739del (DPYD-AS1)
XM_005270562.3:c.2407-93_2407-90del (DPYD) XP_005270619.2:n.2407-93_2407-90del
XM_017000507.1:c.2512-93_2512-90del (DPYD) XP_016855996.1:n.2512-93_2512-90del
XM_017000508.2:c.2128-93_2128-90del (DPYD) XP_016855997.1:n.2128-93_2128-90del
XM_017000509.2:c.2128-93_2128-90del (DPYD) XP_016855998.1:n.2128-93_2128-90del
XM_017000510.1:c.2128-93_2128-90del (DPYD) XP_016855999.1:n.2128-93_2128-90del
NM_000110.4:c.2623-93_2623-90del (DPYD) MANE Select NP_000101.2:n.2623-93_2623-90del
Search 100 bp 5'
Search 100 bp 3'