Canonical Allele Identifier: CA341374877
Gene: DPYD HGNC NCBI
DPYD-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.97564133T>A (hg19) chr1:g.97098577T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97098577T>A , CM000663.2:g.97098577T>A GRCh38
NC_000001.10:g.97564133T>A , CM000663.1:g.97564133T>A GRCh37
NC_000001.9:g.97336721T>A NCBI36
NG_008807.2:g.827483A>T , LRG_722:g.827483A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000370192.8:c.2678A>T (DPYD) MANE Select ENSP00000359211.3:p.Asn893Ile
ENST00000370192.7:c.2678A>T (DPYD) ENSP00000359211.3:p.Asn893Ile
NM_000110.3:c.2678A>T , LRG_722t1:c.2678A>T (DPYD) NP_000101.2:p.Asn893Ile
NR_046590.1:n.64+2591T>A (DPYD-AS1)
XM_005270562.3:c.2462A>T (DPYD) XP_005270619.2:p.Asn821Ile
XM_017000507.1:c.2567A>T (DPYD) XP_016855996.1:p.Asn856Ile
XM_017000508.2:c.2183A>T (DPYD) XP_016855997.1:p.Asn728Ile
XM_017000509.2:c.2183A>T (DPYD) XP_016855998.1:p.Asn728Ile
XM_017000510.1:c.2183A>T (DPYD) XP_016855999.1:p.Asn728Ile
NM_000110.4:c.2678A>T (DPYD) MANE Select NP_000101.2:p.Asn893Ile
Search 100 bp 5'
Search 100 bp 3'