Canonical Allele Identifier: CA1143721855
Gene: DPYD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97691828A= , CM000663.2:g.97691828A= GRCh38
NC_000001.10:g.98157384A= , CM000663.1:g.98157384A= GRCh37
NC_000001.9:g.97929972A= NCBI36
NG_008807.2:g.234232T= , LRG_722:g.234232T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370192.8:c.681-30T= MANE Select ENSP00000359211.3:n.681-30T=
ENST00000370192.7:c.681-30T= ENSP00000359211.3:n.681-30T=
ENST00000474241.1:n.445-30T=
NM_000110.3:c.681-30T= , LRG_722t1:c.681-30T= NP_000101.2:n.681-30T=
XM_005270562.3:c.681-30T= XP_005270619.2:n.681-30T=
XM_006710397.2:c.681-30T= XP_006710460.1:n.681-30T=
XM_006710397.3:c.681-30T= XP_006710460.1:n.681-30T=
XM_017000507.1:c.570-30T= XP_016855996.1:n.570-30T=
XM_017000508.2:c.186-30T= XP_016855997.1:n.186-30T=
XM_017000509.2:c.186-30T= XP_016855998.1:n.186-30T=
XM_017000510.1:c.186-30T= XP_016855999.1:n.186-30T=
NM_000110.4:c.681-30T= MANE Select NP_000101.2:n.681-30T=