Canonical Allele Identifier: CA341376089

Gene: DPYD

Linked Data

• dbSNP Id: rs1676330398
• gnomAD v4: 1-97450144-A-T
• MyVariant Identifiers: chr1:g.97915700A>T (hg19) ; chr1:g.97450144A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97450144A>T , CM000663.2:g.97450144A>T	GRCh38
NC_000001.10:g.97915700A>T , CM000663.1:g.97915700A>T	GRCh37
NC_000001.9:g.97688288A>T	NCBI36
NG_008807.2:g.475916T>A , LRG_722:g.475916T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1820T>A MANE Select	ENSP00000359211.3:p.Phe607Tyr
ENST00000370192.7:c.1820T>A	ENSP00000359211.3:p.Phe607Tyr
NM_000110.3:c.1820T>A , LRG_722t1:c.1820T>A	NP_000101.2:p.Phe607Tyr
XM_005270562.3:c.1604T>A	XP_005270619.2:p.Phe535Tyr
XM_006710397.2:c.1820T>A	XP_006710460.1:p.Phe607Tyr
XM_006710397.3:c.1820T>A	XP_006710460.1:p.Phe607Tyr
XM_017000507.1:c.1709T>A	XP_016855996.1:p.Phe570Tyr
XM_017000508.2:c.1325T>A	XP_016855997.1:p.Phe442Tyr
XM_017000509.2:c.1325T>A	XP_016855998.1:p.Phe442Tyr
XM_017000510.1:c.1325T>A	XP_016855999.1:p.Phe442Tyr
NM_000110.4:c.1820T>A MANE Select	NP_000101.2:p.Phe607Tyr