Canonical Allele Identifier: CA2646706234
Gene: DPYD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97549729_97549730insATATAAGGGGGAA , CM000663.2:g.97549729_97549730insATATAAGGGGGAA GRCh38
NC_000001.10:g.98015285_98015286insATATAAGGGGGAA , CM000663.1:g.98015285_98015286insATATAAGGGGGAA GRCh37
NC_000001.9:g.97787873_97787874insATATAAGGGGGAA NCBI36
NG_008807.2:g.376330_376331insTTCCCCCTTATAT , LRG_722:g.376330_376331insTTCCCCCTTATAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000370192.8:c.1354_1355insTTCCCCCTTATAT MANE Select ENSP00000359211.3:p.Ser452IlefsTer10
ENST00000370192.7:c.1354_1355insTTCCCCCTTATAT ENSP00000359211.3:p.Ser452IlefsTer10
NM_000110.3:c.1354_1355insTTCCCCCTTATAT , LRG_722t1:c.1354_1355insTTCCCCCTTATAT NP_000101.2:p.Ser452IlefsTer10
XM_005270562.3:c.1354_1355insTTCCCCCTTATAT XP_005270619.2:p.Ser452IlefsTer10
XM_006710397.2:c.1354_1355insTTCCCCCTTATAT XP_006710460.1:p.Ser452IlefsTer10
XM_006710397.3:c.1354_1355insTTCCCCCTTATAT XP_006710460.1:p.Ser452IlefsTer10
XM_017000507.1:c.1243_1244insTTCCCCCTTATAT XP_016855996.1:p.Ser415IlefsTer10
XM_017000508.2:c.859_860insTTCCCCCTTATAT XP_016855997.1:p.Ser287IlefsTer10
XM_017000509.2:c.859_860insTTCCCCCTTATAT XP_016855998.1:p.Ser287IlefsTer10
XM_017000510.1:c.859_860insTTCCCCCTTATAT XP_016855999.1:p.Ser287IlefsTer10
NM_000110.4:c.1354_1355insTTCCCCCTTATAT MANE Select NP_000101.2:p.Ser452IlefsTer10