Canonical Allele Identifier: CA2831039306
Gene: DPYD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97515892_97515898delinsGT , CM000663.2:g.97515892_97515898delinsGT GRCh38
NC_000001.10:g.97981448_97981454delinsGT , CM000663.1:g.97981448_97981454delinsGT GRCh37
NC_000001.9:g.97754036_97754042delinsGT NCBI36
NG_008807.2:g.410162_410168delinsAC , LRG_722:g.410162_410168delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000370192.8:c.1568_1574delinsAC MANE Select ENSP00000359211.3:p.Leu523HisfsTer5
ENST00000370192.7:c.1568_1574delinsAC ENSP00000359211.3:p.Leu523HisfsTer5
NM_000110.3:c.1568_1574delinsAC , LRG_722t1:c.1568_1574delinsAC NP_000101.2:p.Leu523HisfsTer5
XM_005270562.3:c.1524+33662_1524+33668delinsAC XP_005270619.2:n.1524+33662_1524+33668delinsAC
XM_006710397.2:c.1568_1574delinsAC XP_006710460.1:p.Leu523HisfsTer5
XM_006710397.3:c.1568_1574delinsAC XP_006710460.1:p.Leu523HisfsTer5
XM_017000507.1:c.1457_1463delinsAC XP_016855996.1:p.Leu486HisfsTer5
XM_017000508.2:c.1073_1079delinsAC XP_016855997.1:p.Leu358HisfsTer5
XM_017000509.2:c.1073_1079delinsAC XP_016855998.1:p.Leu358HisfsTer5
XM_017000510.1:c.1073_1079delinsAC XP_016855999.1:p.Leu358HisfsTer5
NM_000110.4:c.1568_1574delinsAC MANE Select NP_000101.2:p.Leu523HisfsTer5