Canonical Allele Identifier: CA341378245

Gene: DPYD

Linked Data

• dbSNP Id: rs2101975469
• MyVariant Identifiers: chr1:g.97981323C>T (hg19) ; chr1:g.97515767C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97515767C>T , CM000663.2:g.97515767C>T	GRCh38
NC_000001.10:g.97981323C>T , CM000663.1:g.97981323C>T	GRCh37
NC_000001.9:g.97753911C>T	NCBI36
NG_008807.2:g.410293G>A , LRG_722:g.410293G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1699G>A MANE Select	ENSP00000359211.3:p.Gly567Arg
ENST00000370192.7:c.1699G>A	ENSP00000359211.3:p.Gly567Arg
NM_000110.3:c.1699G>A , LRG_722t1:c.1699G>A	NP_000101.2:p.Gly567Arg
XM_005270562.3:c.1524+33793G>A	XP_005270619.2:n.1524+33793G>A
XM_006710397.2:c.1699G>A	XP_006710460.1:p.Gly567Arg
XM_006710397.3:c.1699G>A	XP_006710460.1:p.Gly567Arg
XM_017000507.1:c.1588G>A	XP_016855996.1:p.Gly530Arg
XM_017000508.2:c.1204G>A	XP_016855997.1:p.Gly402Arg
XM_017000509.2:c.1204G>A	XP_016855998.1:p.Gly402Arg
XM_017000510.1:c.1204G>A	XP_016855999.1:p.Gly402Arg
NM_000110.4:c.1699G>A MANE Select	NP_000101.2:p.Gly567Arg