Canonical Allele Identifier: CA341374987
Gene: DPYD HGNC NCBI
DPYD-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.97564186T>A (hg19) chr1:g.97098630T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97098630T>A , CM000663.2:g.97098630T>A GRCh38
NC_000001.10:g.97564186T>A , CM000663.1:g.97564186T>A GRCh37
NC_000001.9:g.97336774T>A NCBI36
NG_008807.2:g.827430A>T , LRG_722:g.827430A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370192.8:c.2625A>T (DPYD) MANE Select ENSP00000359211.3:p.Lys875Asn
ENST00000370192.7:c.2625A>T (DPYD) ENSP00000359211.3:p.Lys875Asn
NM_000110.3:c.2625A>T , LRG_722t1:c.2625A>T (DPYD) NP_000101.2:p.Lys875Asn
NR_046590.1:n.64+2644T>A (DPYD-AS1)
XM_005270562.3:c.2409A>T (DPYD) XP_005270619.2:p.Lys803Asn
XM_017000507.1:c.2514A>T (DPYD) XP_016855996.1:p.Lys838Asn
XM_017000508.2:c.2130A>T (DPYD) XP_016855997.1:p.Lys710Asn
XM_017000509.2:c.2130A>T (DPYD) XP_016855998.1:p.Lys710Asn
XM_017000510.1:c.2130A>T (DPYD) XP_016855999.1:p.Lys710Asn
NM_000110.4:c.2625A>T (DPYD) MANE Select NP_000101.2:p.Lys875Asn
Search 100 bp 5'
Search 100 bp 3'