Canonical Allele Identifier: CA419137419

Gene: DPYD DPYD-AS1

Linked Data

• dbSNP Id: rs1220997866
• gnomAD v2: 1-97770837-T-A
• gnomAD v4: 1-97305281-T-A
• MyVariant Identifiers: chr1:g.97770837T>A (hg19) ; chr1:g.97305281T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97305281T>A , CM000663.2:g.97305281T>A	GRCh38
NC_000001.10:g.97770837T>A , CM000663.1:g.97770837T>A	GRCh37
NC_000001.9:g.97543425T>A	NCBI36
NG_008807.2:g.620779A>T , LRG_722:g.620779A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.2277A>T (DPYD) MANE Select	ENSP00000359211.3:p.Arg759=
ENST00000370192.7:c.2277A>T (DPYD)	ENSP00000359211.3:p.Arg759=
NM_000110.3:c.2277A>T , LRG_722t1:c.2277A>T (DPYD)	NP_000101.2:p.Arg759=
NR_046590.1:n.129-908T>A (DPYD-AS1)
XM_005270562.3:c.2061A>T (DPYD)	XP_005270619.2:p.Arg687=
XM_006710397.2:c.2277A>T (DPYD)	XP_006710460.1:p.Arg759=
XM_006710397.3:c.2277A>T (DPYD)	XP_006710460.1:p.Arg759=
XM_017000507.1:c.2166A>T (DPYD)	XP_016855996.1:p.Arg722=
XM_017000508.2:c.1782A>T (DPYD)	XP_016855997.1:p.Arg594=
XM_017000509.2:c.1782A>T (DPYD)	XP_016855998.1:p.Arg594=
XM_017000510.1:c.1782A>T (DPYD)	XP_016855999.1:p.Arg594=
NM_000110.4:c.2277A>T (DPYD) MANE Select	NP_000101.2:p.Arg759=