Canonical Allele Identifier: CA2744701765
Gene: DPYD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97549501dup , CM000663.2:g.97549501dup GRCh38
NC_000001.10:g.98015057dup , CM000663.1:g.98015057dup GRCh37
NC_000001.9:g.97787645dup NCBI36
NG_008807.2:g.376563dup , LRG_722:g.376563dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000370192.8:c.1524+63dup MANE Select ENSP00000359211.3:n.1524+63dup
ENST00000370192.7:c.1524+63dup ENSP00000359211.3:n.1524+63dup
NM_000110.3:c.1524+63dup , LRG_722t1:c.1524+63dup NP_000101.2:n.1524+63dup
XM_005270562.3:c.1524+63dup XP_005270619.2:n.1524+63dup
XM_006710397.2:c.1524+63dup XP_006710460.1:n.1524+63dup
XM_006710397.3:c.1524+63dup XP_006710460.1:n.1524+63dup
XM_017000507.1:c.1413+63dup XP_016855996.1:n.1413+63dup
XM_017000508.2:c.1029+63dup XP_016855997.1:n.1029+63dup
XM_017000509.2:c.1029+63dup XP_016855998.1:n.1029+63dup
XM_017000510.1:c.1029+63dup XP_016855999.1:n.1029+63dup
NM_000110.4:c.1524+63dup MANE Select NP_000101.2:n.1524+63dup