Canonical Allele Identifier: CA2646705218
Gene: DPYD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97382470dup , CM000663.2:g.97382470dup GRCh38
NC_000001.10:g.97848026dup , CM000663.1:g.97848026dup GRCh37
NC_000001.9:g.97620614dup NCBI36
NG_008807.2:g.543594dup , LRG_722:g.543594dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000370192.8:c.1906-5dup MANE Select ENSP00000359211.3:n.1906-5dup
ENST00000370192.7:c.1906-5dup ENSP00000359211.3:n.1906-5dup
NM_000110.3:c.1906-5dup , LRG_722t1:c.1906-5dup NP_000101.2:n.1906-5dup
XM_005270562.3:c.1690-5dup XP_005270619.2:n.1690-5dup
XM_006710397.2:c.1906-5dup XP_006710460.1:n.1906-5dup
XR_947619.1:n.1347-1164dup
XR_947620.1:n.1125-1164dup
XR_947621.1:n.1347-1164dup
XM_006710397.3:c.1906-5dup XP_006710460.1:n.1906-5dup
XM_017000507.1:c.1795-5dup XP_016855996.1:n.1795-5dup
XM_017000508.2:c.1411-5dup XP_016855997.1:n.1411-5dup
XM_017000509.2:c.1411-5dup XP_016855998.1:n.1411-5dup
XM_017000510.1:c.1411-5dup XP_016855999.1:n.1411-5dup
XR_001737686.2:n.692-1164dup
XR_001737687.1:n.692-1164dup
XR_001737688.2:n.692-1164dup
NM_000110.4:c.1906-5dup MANE Select NP_000101.2:n.1906-5dup