Canonical Allele Identifier: CA341379334
Gene: DPYD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97691788T>C , CM000663.2:g.97691788T>C GRCh38
NC_000001.10:g.98157344T>C , CM000663.1:g.98157344T>C GRCh37
NC_000001.9:g.97929932T>C NCBI36
NG_008807.2:g.234272A>G , LRG_722:g.234272A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000370192.8:c.691A>G MANE Select ENSP00000359211.3:p.Ile231Val
ENST00000370192.7:c.691A>G ENSP00000359211.3:p.Ile231Val
ENST00000474241.1:n.455A>G
NM_000110.3:c.691A>G , LRG_722t1:c.691A>G NP_000101.2:p.Ile231Val
XM_005270562.3:c.691A>G XP_005270619.2:p.Ile231Val
XM_006710397.2:c.691A>G XP_006710460.1:p.Ile231Val
XM_006710397.3:c.691A>G XP_006710460.1:p.Ile231Val
XM_017000507.1:c.580A>G XP_016855996.1:p.Ile194Val
XM_017000508.2:c.196A>G XP_016855997.1:p.Ile66Val
XM_017000509.2:c.196A>G XP_016855998.1:p.Ile66Val
XM_017000510.1:c.196A>G XP_016855999.1:p.Ile66Val
NM_000110.4:c.691A>G MANE Select NP_000101.2:p.Ile231Val