Canonical Allele Identifier: CA419145476
Gene: DPYD HGNC NCBI

Linked Data

dbSNP Id: rs1235826119
MyVariant Identifiers: chr1:g.97915666A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97450110A>T , CM000663.2:g.97450110A>T GRCh38
NC_000001.10:g.97915666A>T , CM000663.1:g.97915666A>T GRCh37
NC_000001.9:g.97688254A>T NCBI36
NG_008807.2:g.475950T>A , LRG_722:g.475950T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000370192.8:c.1854T>A MANE Select ENSP00000359211.3:p.Ala618=
ENST00000370192.7:c.1854T>A ENSP00000359211.3:p.Ala618=
NM_000110.3:c.1854T>A , LRG_722t1:c.1854T>A NP_000101.2:p.Ala618=
XM_005270562.3:c.1638T>A XP_005270619.2:p.Ala546=
XM_006710397.2:c.1854T>A XP_006710460.1:p.Ala618=
XM_006710397.3:c.1854T>A XP_006710460.1:p.Ala618=
XM_017000507.1:c.1743T>A XP_016855996.1:p.Ala581=
XM_017000508.2:c.1359T>A XP_016855997.1:p.Ala453=
XM_017000509.2:c.1359T>A XP_016855998.1:p.Ala453=
XM_017000510.1:c.1359T>A XP_016855999.1:p.Ala453=
NM_000110.4:c.1854T>A MANE Select NP_000101.2:p.Ala618=