Canonical Allele Identifier: CA341375934
Gene: DPYD HGNC NCBI

Linked Data

dbSNP Id: rs1170223787

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97450075G>A , CM000663.2:g.97450075G>A GRCh38
NC_000001.10:g.97915631G>A , CM000663.1:g.97915631G>A GRCh37
NC_000001.9:g.97688219G>A NCBI36
NG_008807.2:g.475985C>T , LRG_722:g.475985C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370192.8:c.1889C>T MANE Select ENSP00000359211.3:p.Ala630Val
ENST00000370192.7:c.1889C>T ENSP00000359211.3:p.Ala630Val
NM_000110.3:c.1889C>T , LRG_722t1:c.1889C>T NP_000101.2:p.Ala630Val
XM_005270562.3:c.1673C>T XP_005270619.2:p.Ala558Val
XM_006710397.2:c.1889C>T XP_006710460.1:p.Ala630Val
XM_006710397.3:c.1889C>T XP_006710460.1:p.Ala630Val
XM_017000507.1:c.1778C>T XP_016855996.1:p.Ala593Val
XM_017000508.2:c.1394C>T XP_016855997.1:p.Ala465Val
XM_017000509.2:c.1394C>T XP_016855998.1:p.Ala465Val
XM_017000510.1:c.1394C>T XP_016855999.1:p.Ala465Val
NM_000110.4:c.1889C>T MANE Select NP_000101.2:p.Ala630Val