Canonical Allele Identifier: CA341376061
Gene: DPYD HGNC NCBI

Linked Data

dbSNP Id: rs1676329391

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97450131C>G , CM000663.2:g.97450131C>G GRCh38
NC_000001.10:g.97915687C>G , CM000663.1:g.97915687C>G GRCh37
NC_000001.9:g.97688275C>G NCBI36
NG_008807.2:g.475929G>C , LRG_722:g.475929G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000370192.8:c.1833G>C MANE Select ENSP00000359211.3:p.Glu611Asp
ENST00000370192.7:c.1833G>C ENSP00000359211.3:p.Glu611Asp
NM_000110.3:c.1833G>C , LRG_722t1:c.1833G>C NP_000101.2:p.Glu611Asp
XM_005270562.3:c.1617G>C XP_005270619.2:p.Glu539Asp
XM_006710397.2:c.1833G>C XP_006710460.1:p.Glu611Asp
XM_006710397.3:c.1833G>C XP_006710460.1:p.Glu611Asp
XM_017000507.1:c.1722G>C XP_016855996.1:p.Glu574Asp
XM_017000508.2:c.1338G>C XP_016855997.1:p.Glu446Asp
XM_017000509.2:c.1338G>C XP_016855998.1:p.Glu446Asp
XM_017000510.1:c.1338G>C XP_016855999.1:p.Glu446Asp
NM_000110.4:c.1833G>C MANE Select NP_000101.2:p.Glu611Asp