Canonical Allele Identifier: CA2992398435
Gene: DPYD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97691790dup , CM000663.2:g.97691790dup GRCh38
NC_000001.10:g.98157346dup , CM000663.1:g.98157346dup GRCh37
NC_000001.9:g.97929934dup NCBI36
NG_008807.2:g.234272dup , LRG_722:g.234272dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000370192.8:c.691dup MANE Select ENSP00000359211.3:p.Ile231AsnfsTer9
ENST00000370192.7:c.691dup ENSP00000359211.3:p.Ile231AsnfsTer9
ENST00000474241.1:n.455dup
NM_000110.3:c.691dup , LRG_722t1:c.691dup NP_000101.2:p.Ile231AsnfsTer9
XM_005270562.3:c.691dup XP_005270619.2:p.Ile231AsnfsTer9
XM_006710397.2:c.691dup XP_006710460.1:p.Ile231AsnfsTer9
XM_006710397.3:c.691dup XP_006710460.1:p.Ile231AsnfsTer9
XM_017000507.1:c.580dup XP_016855996.1:p.Ile194AsnfsTer9
XM_017000508.2:c.196dup XP_016855997.1:p.Ile66AsnfsTer9
XM_017000509.2:c.196dup XP_016855998.1:p.Ile66AsnfsTer9
XM_017000510.1:c.196dup XP_016855999.1:p.Ile66AsnfsTer9
NM_000110.4:c.691dup MANE Select NP_000101.2:p.Ile231AsnfsTer9