Canonical Allele Identifier: CA963571
Gene: DPYD HGNC NCBI

Linked Data

dbSNP Id: rs751418176

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97691709dup , CM000663.2:g.97691709dup GRCh38
NC_000001.10:g.98157265dup , CM000663.1:g.98157265dup GRCh37
NC_000001.9:g.97929853dup NCBI36
NG_008807.2:g.234357dup , LRG_722:g.234357dup

Transcript Alleles

HGVS Amino-acid change
ENST00000370192.8:c.762+14dup MANE Select ENSP00000359211.3:n.762+14dup
ENST00000370192.7:c.762+14dup ENSP00000359211.3:n.762+14dup
ENST00000474241.1:n.540dup
NM_000110.3:c.762+14dup , LRG_722t1:c.762+14dup NP_000101.2:n.762+14dup
XM_005270562.3:c.762+14dup XP_005270619.2:n.762+14dup
XM_006710397.2:c.762+14dup XP_006710460.1:n.762+14dup
XM_006710397.3:c.762+14dup XP_006710460.1:n.762+14dup
XM_017000507.1:c.651+14dup XP_016855996.1:n.651+14dup
XM_017000508.2:c.267+14dup XP_016855997.1:n.267+14dup
XM_017000509.2:c.267+14dup XP_016855998.1:n.267+14dup
XM_017000510.1:c.267+14dup XP_016855999.1:n.267+14dup
NM_000110.4:c.762+14dup MANE Select NP_000101.2:n.762+14dup