Canonical Allele Identifier: CA341379256
Gene: DPYD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97691751A>G , CM000663.2:g.97691751A>G GRCh38
NC_000001.10:g.98157307A>G , CM000663.1:g.98157307A>G GRCh37
NC_000001.9:g.97929895A>G NCBI36
NG_008807.2:g.234309T>C , LRG_722:g.234309T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000370192.8:c.728T>C MANE Select ENSP00000359211.3:p.Phe243Ser
ENST00000370192.7:c.728T>C ENSP00000359211.3:p.Phe243Ser
ENST00000474241.1:n.492T>C
NM_000110.3:c.728T>C , LRG_722t1:c.728T>C NP_000101.2:p.Phe243Ser
XM_005270562.3:c.728T>C XP_005270619.2:p.Phe243Ser
XM_006710397.2:c.728T>C XP_006710460.1:p.Phe243Ser
XM_006710397.3:c.728T>C XP_006710460.1:p.Phe243Ser
XM_017000507.1:c.617T>C XP_016855996.1:p.Phe206Ser
XM_017000508.2:c.233T>C XP_016855997.1:p.Phe78Ser
XM_017000509.2:c.233T>C XP_016855998.1:p.Phe78Ser
XM_017000510.1:c.233T>C XP_016855999.1:p.Phe78Ser
NM_000110.4:c.728T>C MANE Select NP_000101.2:p.Phe243Ser