Canonical Allele Identifier: CA962969
Gene: DPYD HGNC NCBI
DPYD-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2674942
ClinVar RCV Id: RCV003467852
dbSNP Id: rs771839581
ExAC: 1:97564158 G / A
gnomAD v2: 1-97564158-G-A
gnomAD v3: 1-97098602-G-A
gnomAD v4: 1-97098602-G-A
MyVariant Identifiers: chr1:g.97564158G>A (hg19) chr1:g.97098602G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97098602G>A , CM000663.2:g.97098602G>A GRCh38
NC_000001.10:g.97564158G>A , CM000663.1:g.97564158G>A GRCh37
NC_000001.9:g.97336746G>A NCBI36
NG_008807.2:g.827458C>T , LRG_722:g.827458C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370192.8:c.2653C>T (DPYD) MANE Select ENSP00000359211.3:p.Gln885Ter
ENST00000370192.7:c.2653C>T (DPYD) ENSP00000359211.3:p.Gln885Ter
NM_000110.3:c.2653C>T , LRG_722t1:c.2653C>T (DPYD) NP_000101.2:p.Gln885Ter
NR_046590.1:n.64+2616G>A (DPYD-AS1)
XM_005270562.3:c.2437C>T (DPYD) XP_005270619.2:p.Gln813Ter
XM_017000507.1:c.2542C>T (DPYD) XP_016855996.1:p.Gln848Ter
XM_017000508.2:c.2158C>T (DPYD) XP_016855997.1:p.Gln720Ter
XM_017000509.2:c.2158C>T (DPYD) XP_016855998.1:p.Gln720Ter
XM_017000510.1:c.2158C>T (DPYD) XP_016855999.1:p.Gln720Ter
NM_000110.4:c.2653C>T (DPYD) MANE Select NP_000101.2:p.Gln885Ter
Search 100 bp 5'
Search 100 bp 3'