Canonical Allele Identifier: CA963015
Gene: DPYD HGNC NCBI
DPYD-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs748214188
gnomAD v2: 1-97658737-A-T
gnomAD v4: 1-97193181-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97193181A>T , CM000663.2:g.97193181A>T GRCh38
NC_000001.10:g.97658737A>T , CM000663.1:g.97658737A>T GRCh37
NC_000001.9:g.97431325A>T NCBI36
NG_008807.2:g.732879T>A , LRG_722:g.732879T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370192.8:c.2510T>A (DPYD) MANE Select ENSP00000359211.3:p.Leu837Gln
ENST00000370192.7:c.2510T>A (DPYD) ENSP00000359211.3:p.Leu837Gln
NM_000110.3:c.2510T>A , LRG_722t1:c.2510T>A (DPYD) NP_000101.2:p.Leu837Gln
NR_046590.1:n.65-72233A>T (DPYD-AS1)
XM_005270562.3:c.2294T>A (DPYD) XP_005270619.2:p.Leu765Gln
XM_006710397.2:c.2510T>A (DPYD) XP_006710460.1:p.Leu837Gln
XM_006710397.3:c.2510T>A (DPYD) XP_006710460.1:p.Leu837Gln
XM_017000507.1:c.2399T>A (DPYD) XP_016855996.1:p.Leu800Gln
XM_017000508.2:c.2015T>A (DPYD) XP_016855997.1:p.Leu672Gln
XM_017000509.2:c.2015T>A (DPYD) XP_016855998.1:p.Leu672Gln
XM_017000510.1:c.2015T>A (DPYD) XP_016855999.1:p.Leu672Gln
NM_000110.4:c.2510T>A (DPYD) MANE Select NP_000101.2:p.Leu837Gln