Canonical Allele Identifier: CA341374907

Gene: DPYD DPYD-AS1

Linked Data

• dbSNP Id: rs1570450908
• gnomAD v4: 1-97098590-T-C
• MyVariant Identifiers: chr1:g.97564146T>C (hg19) ; chr1:g.97098590T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97098590T>C , CM000663.2:g.97098590T>C	GRCh38
NC_000001.10:g.97564146T>C , CM000663.1:g.97564146T>C	GRCh37
NC_000001.9:g.97336734T>C	NCBI36
NG_008807.2:g.827470A>G , LRG_722:g.827470A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2665A>G (DPYD) MANE Select	ENSP00000359211.3:p.Ile889Val
ENST00000370192.7:c.2665A>G (DPYD)	ENSP00000359211.3:p.Ile889Val
NM_000110.3:c.2665A>G , LRG_722t1:c.2665A>G (DPYD)	NP_000101.2:p.Ile889Val
NR_046590.1:n.64+2604T>C (DPYD-AS1)
XM_005270562.3:c.2449A>G (DPYD)	XP_005270619.2:p.Ile817Val
XM_017000507.1:c.2554A>G (DPYD)	XP_016855996.1:p.Ile852Val
XM_017000508.2:c.2170A>G (DPYD)	XP_016855997.1:p.Ile724Val
XM_017000509.2:c.2170A>G (DPYD)	XP_016855998.1:p.Ile724Val
XM_017000510.1:c.2170A>G (DPYD)	XP_016855999.1:p.Ile724Val
NM_000110.4:c.2665A>G (DPYD) MANE Select	NP_000101.2:p.Ile889Val