Canonical Allele Identifier: CA2646703354
Gene: DPYD HGNC NCBI
DPYD-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs2101594756
gnomAD v4: 1-97098401-AC-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97098402del , CM000663.2:g.97098402del GRCh38
NC_000001.10:g.97563958del , CM000663.1:g.97563958del GRCh37
NC_000001.9:g.97336546del NCBI36
NG_008807.2:g.827658del , LRG_722:g.827658del

Transcript Alleles

HGVS Amino-acid Change
ENST00000370192.8:c.2766+87del (DPYD) MANE Select ENSP00000359211.3:n.2766+87del
ENST00000370192.7:c.2766+87del (DPYD) ENSP00000359211.3:n.2766+87del
NM_000110.3:c.2766+87del , LRG_722t1:c.2766+87del (DPYD) NP_000101.2:n.2766+87del
NR_046590.1:n.64+2416del (DPYD-AS1)
XM_005270562.3:c.2550+87del (DPYD) XP_005270619.2:n.2550+87del
XM_017000507.1:c.2655+87del (DPYD) XP_016855996.1:n.2655+87del
XM_017000508.2:c.2271+87del (DPYD) XP_016855997.1:n.2271+87del
XM_017000509.2:c.2271+87del (DPYD) XP_016855998.1:n.2271+87del
XM_017000510.1:c.2271+87del (DPYD) XP_016855999.1:n.2271+87del
NM_000110.4:c.2766+87del (DPYD) MANE Select NP_000101.2:n.2766+87del
Search 100 bp 5'
Search 100 bp 3'