Canonical Allele Identifier: CA341377806
Gene: DPYD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97549688G>C , CM000663.2:g.97549688G>C GRCh38
NC_000001.10:g.98015244G>C , CM000663.1:g.98015244G>C GRCh37
NC_000001.9:g.97787832G>C NCBI36
NG_008807.2:g.376372C>G , LRG_722:g.376372C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370192.8:c.1396C>G MANE Select ENSP00000359211.3:p.Pro466Ala
ENST00000370192.7:c.1396C>G ENSP00000359211.3:p.Pro466Ala
NM_000110.3:c.1396C>G , LRG_722t1:c.1396C>G NP_000101.2:p.Pro466Ala
XM_005270562.3:c.1396C>G XP_005270619.2:p.Pro466Ala
XM_006710397.2:c.1396C>G XP_006710460.1:p.Pro466Ala
XM_006710397.3:c.1396C>G XP_006710460.1:p.Pro466Ala
XM_017000507.1:c.1285C>G XP_016855996.1:p.Pro429Ala
XM_017000508.2:c.901C>G XP_016855997.1:p.Pro301Ala
XM_017000509.2:c.901C>G XP_016855998.1:p.Pro301Ala
XM_017000510.1:c.901C>G XP_016855999.1:p.Pro301Ala
NM_000110.4:c.1396C>G MANE Select NP_000101.2:p.Pro466Ala