Canonical Allele Identifier: CA419137008
Gene: DPYD HGNC NCBI
DPYD-AS1 HGNC NCBI

Linked Data

COSMIC: COSM3493626
MyVariant Identifiers: chr1:g.97564144G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97098588G>A , CM000663.2:g.97098588G>A GRCh38
NC_000001.10:g.97564144G>A , CM000663.1:g.97564144G>A GRCh37
NC_000001.9:g.97336732G>A NCBI36
NG_008807.2:g.827472C>T , LRG_722:g.827472C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370192.8:c.2667C>T (DPYD) MANE Select ENSP00000359211.3:p.Ile889=
ENST00000370192.7:c.2667C>T (DPYD) ENSP00000359211.3:p.Ile889=
NM_000110.3:c.2667C>T , LRG_722t1:c.2667C>T (DPYD) NP_000101.2:p.Ile889=
NR_046590.1:n.64+2602G>A (DPYD-AS1)
XM_005270562.3:c.2451C>T (DPYD) XP_005270619.2:p.Ile817=
XM_017000507.1:c.2556C>T (DPYD) XP_016855996.1:p.Ile852=
XM_017000508.2:c.2172C>T (DPYD) XP_016855997.1:p.Ile724=
XM_017000509.2:c.2172C>T (DPYD) XP_016855998.1:p.Ile724=
XM_017000510.1:c.2172C>T (DPYD) XP_016855999.1:p.Ile724=
NM_000110.4:c.2667C>T (DPYD) MANE Select NP_000101.2:p.Ile889=
Search 100 bp 5'
Search 100 bp 3'