Canonical Allele Identifier: CA2646703863
Gene: DPYD HGNC NCBI
DPYD-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97234902_97234903del , CM000663.2:g.97234902_97234903del GRCh38
NC_000001.10:g.97700458_97700459del , CM000663.1:g.97700458_97700459del GRCh37
NC_000001.9:g.97473046_97473047del NCBI36
NG_008807.2:g.691159_691160del , LRG_722:g.691159_691160del

Transcript Alleles

HGVS Amino-acid Change
ENST00000370192.8:c.2393_2394del (DPYD) MANE Select ENSP00000359211.3:p.Ser798CysfsTer2
ENST00000370192.7:c.2393_2394del (DPYD) ENSP00000359211.3:p.Ser798CysfsTer2
NM_000110.3:c.2393_2394del , LRG_722t1:c.2393_2394del (DPYD) NP_000101.2:p.Ser798CysfsTer2
NR_046590.1:n.65-30512_65-30511del (DPYD-AS1)
XM_005270562.3:c.2177_2178del (DPYD) XP_005270619.2:p.Ser726CysfsTer2
XM_006710397.2:c.2393_2394del (DPYD) XP_006710460.1:p.Ser798CysfsTer2
XM_006710397.3:c.2393_2394del (DPYD) XP_006710460.1:p.Ser798CysfsTer2
XM_017000507.1:c.2282_2283del (DPYD) XP_016855996.1:p.Ser761CysfsTer2
XM_017000508.2:c.1898_1899del (DPYD) XP_016855997.1:p.Ser633CysfsTer2
XM_017000509.2:c.1898_1899del (DPYD) XP_016855998.1:p.Ser633CysfsTer2
XM_017000510.1:c.1898_1899del (DPYD) XP_016855999.1:p.Ser633CysfsTer2
NM_000110.4:c.2393_2394del (DPYD) MANE Select NP_000101.2:p.Ser798CysfsTer2