Canonical Allele Identifier: CA2602270155
Gene: DPYD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97382521_97382526del , CM000663.2:g.97382521_97382526del GRCh38
NC_000001.10:g.97848077_97848082del , CM000663.1:g.97848077_97848082del GRCh37
NC_000001.9:g.97620665_97620670del NCBI36
NG_008807.2:g.543534_543539del , LRG_722:g.543534_543539del

Transcript Alleles

HGVS Amino-acid Change
ENST00000370192.8:c.1906-65_1906-60del MANE Select ENSP00000359211.3:n.1906-65_1906-60del
ENST00000370192.7:c.1906-65_1906-60del ENSP00000359211.3:n.1906-65_1906-60del
NM_000110.3:c.1906-65_1906-60del , LRG_722t1:c.1906-65_1906-60del NP_000101.2:n.1906-65_1906-60del
XM_005270562.3:c.1690-65_1690-60del XP_005270619.2:n.1690-65_1690-60del
XM_006710397.2:c.1906-65_1906-60del XP_006710460.1:n.1906-65_1906-60del
XR_947619.1:n.1347-1113_1347-1108del
XR_947620.1:n.1125-1113_1125-1108del
XR_947621.1:n.1347-1113_1347-1108del
XM_006710397.3:c.1906-65_1906-60del XP_006710460.1:n.1906-65_1906-60del
XM_017000507.1:c.1795-65_1795-60del XP_016855996.1:n.1795-65_1795-60del
XM_017000508.2:c.1411-65_1411-60del XP_016855997.1:n.1411-65_1411-60del
XM_017000509.2:c.1411-65_1411-60del XP_016855998.1:n.1411-65_1411-60del
XM_017000510.1:c.1411-65_1411-60del XP_016855999.1:n.1411-65_1411-60del
XR_001737686.2:n.692-1113_692-1108del
XR_001737687.1:n.692-1113_692-1108del
XR_001737688.2:n.692-1113_692-1108del
NM_000110.4:c.1906-65_1906-60del MANE Select NP_000101.2:n.1906-65_1906-60del