Canonical Allele Identifier: CA1182979301
Gene: DPYD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97691712T= , CM000663.2:g.97691712T= GRCh38
NC_000001.10:g.98157268T= , CM000663.1:g.98157268T= GRCh37
NC_000001.9:g.97929856T= NCBI36
NG_008807.2:g.234348A= , LRG_722:g.234348A=

Transcript Alleles

HGVS Amino-acid change
ENST00000370192.8:c.762+5A= MANE Select ENSP00000359211.3:n.762+5A=
ENST00000370192.7:c.762+5A= ENSP00000359211.3:n.762+5A=
ENST00000474241.1:n.531A=
NM_000110.3:c.762+5A= , LRG_722t1:c.762+5A= NP_000101.2:n.762+5A=
XM_005270562.3:c.762+5A= XP_005270619.2:n.762+5A=
XM_006710397.2:c.762+5A= XP_006710460.1:n.762+5A=
XM_006710397.3:c.762+5A= XP_006710460.1:n.762+5A=
XM_017000507.1:c.651+5A= XP_016855996.1:n.651+5A=
XM_017000508.2:c.267+5A= XP_016855997.1:n.267+5A=
XM_017000509.2:c.267+5A= XP_016855998.1:n.267+5A=
XM_017000510.1:c.267+5A= XP_016855999.1:n.267+5A=
NM_000110.4:c.762+5A= MANE Select NP_000101.2:n.762+5A=