Canonical Allele Identifier: CA2574442029
Gene: DPYD HGNC NCBI
DPYD-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97193310_97193311dup , CM000663.2:g.97193310_97193311dup GRCh38
NC_000001.10:g.97658866_97658867dup , CM000663.1:g.97658866_97658867dup GRCh37
NC_000001.9:g.97431454_97431455dup NCBI36
NG_008807.2:g.732750_732751dup , LRG_722:g.732750_732751dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000370192.8:c.2443-62_2443-61dup (DPYD) MANE Select ENSP00000359211.3:n.2443-62_2443-61dup
ENST00000370192.7:c.2443-62_2443-61dup (DPYD) ENSP00000359211.3:n.2443-62_2443-61dup
NM_000110.3:c.2443-62_2443-61dup , LRG_722t1:c.2443-62_2443-61dup (DPYD) NP_000101.2:n.2443-62_2443-61dup
NR_046590.1:n.65-72104_65-72103dup (DPYD-AS1)
XM_005270562.3:c.2227-62_2227-61dup (DPYD) XP_005270619.2:n.2227-62_2227-61dup
XM_006710397.2:c.2443-62_2443-61dup (DPYD) XP_006710460.1:n.2443-62_2443-61dup
XM_006710397.3:c.2443-62_2443-61dup (DPYD) XP_006710460.1:n.2443-62_2443-61dup
XM_017000507.1:c.2332-62_2332-61dup (DPYD) XP_016855996.1:n.2332-62_2332-61dup
XM_017000508.2:c.1948-62_1948-61dup (DPYD) XP_016855997.1:n.1948-62_1948-61dup
XM_017000509.2:c.1948-62_1948-61dup (DPYD) XP_016855998.1:n.1948-62_1948-61dup
XM_017000510.1:c.1948-62_1948-61dup (DPYD) XP_016855999.1:n.1948-62_1948-61dup
NM_000110.4:c.2443-62_2443-61dup (DPYD) MANE Select NP_000101.2:n.2443-62_2443-61dup