Canonical Allele Identifier: CA419137025
Gene: DPYD HGNC NCBI
DPYD-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.97564171T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97098615T>A , CM000663.2:g.97098615T>A GRCh38
NC_000001.10:g.97564171T>A , CM000663.1:g.97564171T>A GRCh37
NC_000001.9:g.97336759T>A NCBI36
NG_008807.2:g.827445A>T , LRG_722:g.827445A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370192.8:c.2640A>T (DPYD) MANE Select ENSP00000359211.3:p.Gly880=
ENST00000370192.7:c.2640A>T (DPYD) ENSP00000359211.3:p.Gly880=
NM_000110.3:c.2640A>T , LRG_722t1:c.2640A>T (DPYD) NP_000101.2:p.Gly880=
NR_046590.1:n.64+2629T>A (DPYD-AS1)
XM_005270562.3:c.2424A>T (DPYD) XP_005270619.2:p.Gly808=
XM_017000507.1:c.2529A>T (DPYD) XP_016855996.1:p.Gly843=
XM_017000508.2:c.2145A>T (DPYD) XP_016855997.1:p.Gly715=
XM_017000509.2:c.2145A>T (DPYD) XP_016855998.1:p.Gly715=
XM_017000510.1:c.2145A>T (DPYD) XP_016855999.1:p.Gly715=
NM_000110.4:c.2640A>T (DPYD) MANE Select NP_000101.2:p.Gly880=