Canonical Allele Identifier: CA2646706262
Gene: DPYD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97549824dup , CM000663.2:g.97549824dup GRCh38
NC_000001.10:g.98015380dup , CM000663.1:g.98015380dup GRCh37
NC_000001.9:g.97787968dup NCBI36
NG_008807.2:g.376240dup , LRG_722:g.376240dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000370192.8:c.1340-76dup MANE Select ENSP00000359211.3:n.1340-76dup
ENST00000370192.7:c.1340-76dup ENSP00000359211.3:n.1340-76dup
NM_000110.3:c.1340-76dup , LRG_722t1:c.1340-76dup NP_000101.2:n.1340-76dup
XM_005270562.3:c.1340-76dup XP_005270619.2:n.1340-76dup
XM_006710397.2:c.1340-76dup XP_006710460.1:n.1340-76dup
XM_006710397.3:c.1340-76dup XP_006710460.1:n.1340-76dup
XM_017000507.1:c.1229-76dup XP_016855996.1:n.1229-76dup
XM_017000508.2:c.845-76dup XP_016855997.1:n.845-76dup
XM_017000509.2:c.845-76dup XP_016855998.1:n.845-76dup
XM_017000510.1:c.845-76dup XP_016855999.1:n.845-76dup
NM_000110.4:c.1340-76dup MANE Select NP_000101.2:n.1340-76dup