Canonical Allele Identifier: CA341377444
Gene: DPYD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97549588G>C , CM000663.2:g.97549588G>C GRCh38
NC_000001.10:g.98015144G>C , CM000663.1:g.98015144G>C GRCh37
NC_000001.9:g.97787732G>C NCBI36
NG_008807.2:g.376472C>G , LRG_722:g.376472C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370192.8:c.1496C>G MANE Select ENSP00000359211.3:p.Ala499Gly
ENST00000370192.7:c.1496C>G ENSP00000359211.3:p.Ala499Gly
NM_000110.3:c.1496C>G , LRG_722t1:c.1496C>G NP_000101.2:p.Ala499Gly
XM_005270562.3:c.1496C>G XP_005270619.2:p.Ala499Gly
XM_006710397.2:c.1496C>G XP_006710460.1:p.Ala499Gly
XM_006710397.3:c.1496C>G XP_006710460.1:p.Ala499Gly
XM_017000507.1:c.1385C>G XP_016855996.1:p.Ala462Gly
XM_017000508.2:c.1001C>G XP_016855997.1:p.Ala334Gly
XM_017000509.2:c.1001C>G XP_016855998.1:p.Ala334Gly
XM_017000510.1:c.1001C>G XP_016855999.1:p.Ala334Gly
NM_000110.4:c.1496C>G MANE Select NP_000101.2:p.Ala499Gly