Canonical Allele Identifier: CA341373583

Gene: DPYD DPYD-AS1

Linked Data

• dbSNP Id: rs1658507674
• gnomAD v4: 1-97193215-C-T
• MyVariant Identifiers: chr1:g.97658771C>T (hg19) ; chr1:g.97193215C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97193215C>T , CM000663.2:g.97193215C>T	GRCh38
NC_000001.10:g.97658771C>T , CM000663.1:g.97658771C>T	GRCh37
NC_000001.9:g.97431359C>T	NCBI36
NG_008807.2:g.732845G>A , LRG_722:g.732845G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2476G>A (DPYD) MANE Select	ENSP00000359211.3:p.Val826Met
ENST00000370192.7:c.2476G>A (DPYD)	ENSP00000359211.3:p.Val826Met
NM_000110.3:c.2476G>A , LRG_722t1:c.2476G>A (DPYD)	NP_000101.2:p.Val826Met
NR_046590.1:n.65-72199C>T (DPYD-AS1)
XM_005270562.3:c.2260G>A (DPYD)	XP_005270619.2:p.Val754Met
XM_006710397.2:c.2476G>A (DPYD)	XP_006710460.1:p.Val826Met
XM_006710397.3:c.2476G>A (DPYD)	XP_006710460.1:p.Val826Met
XM_017000507.1:c.2365G>A (DPYD)	XP_016855996.1:p.Val789Met
XM_017000508.2:c.1981G>A (DPYD)	XP_016855997.1:p.Val661Met
XM_017000509.2:c.1981G>A (DPYD)	XP_016855998.1:p.Val661Met
XM_017000510.1:c.1981G>A (DPYD)	XP_016855999.1:p.Val661Met
NM_000110.4:c.2476G>A (DPYD) MANE Select	NP_000101.2:p.Val826Met