Canonical Allele Identifier: CA341375024

Gene: DPYD DPYD-AS1

Linked Data

• dbSNP Id: rs2101035587
• MyVariant Identifiers: chr1:g.97770824C>T (hg19) ; chr1:g.97305268C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97305268C>T , CM000663.2:g.97305268C>T	GRCh38
NC_000001.10:g.97770824C>T , CM000663.1:g.97770824C>T	GRCh37
NC_000001.9:g.97543412C>T	NCBI36
NG_008807.2:g.620792G>A , LRG_722:g.620792G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.2290G>A (DPYD) MANE Select	ENSP00000359211.3:p.Gly764Arg
ENST00000370192.7:c.2290G>A (DPYD)	ENSP00000359211.3:p.Gly764Arg
NM_000110.3:c.2290G>A , LRG_722t1:c.2290G>A (DPYD)	NP_000101.2:p.Gly764Arg
NR_046590.1:n.129-921C>T (DPYD-AS1)
XM_005270562.3:c.2074G>A (DPYD)	XP_005270619.2:p.Gly692Arg
XM_006710397.2:c.2290G>A (DPYD)	XP_006710460.1:p.Gly764Arg
XM_006710397.3:c.2290G>A (DPYD)	XP_006710460.1:p.Gly764Arg
XM_017000507.1:c.2179G>A (DPYD)	XP_016855996.1:p.Gly727Arg
XM_017000508.2:c.1795G>A (DPYD)	XP_016855997.1:p.Gly599Arg
XM_017000509.2:c.1795G>A (DPYD)	XP_016855998.1:p.Gly599Arg
XM_017000510.1:c.1795G>A (DPYD)	XP_016855999.1:p.Gly599Arg
NM_000110.4:c.2290G>A (DPYD) MANE Select	NP_000101.2:p.Gly764Arg