Canonical Allele Identifier: CA419137422

Gene: DPYD DPYD-AS1

Linked Data

• dbSNP Id: rs759372918
• gnomAD v4: 1-97305283-G-T
• MyVariant Identifiers: chr1:g.97770839G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97305283G>T , CM000663.2:g.97305283G>T	GRCh38
NC_000001.10:g.97770839G>T , CM000663.1:g.97770839G>T	GRCh37
NC_000001.9:g.97543427G>T	NCBI36
NG_008807.2:g.620777C>A , LRG_722:g.620777C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2275C>A (DPYD) MANE Select	ENSP00000359211.3:p.Arg759=
ENST00000370192.7:c.2275C>A (DPYD)	ENSP00000359211.3:p.Arg759=
NM_000110.3:c.2275C>A , LRG_722t1:c.2275C>A (DPYD)	NP_000101.2:p.Arg759=
NR_046590.1:n.129-906G>T (DPYD-AS1)
XM_005270562.3:c.2059C>A (DPYD)	XP_005270619.2:p.Arg687=
XM_006710397.2:c.2275C>A (DPYD)	XP_006710460.1:p.Arg759=
XM_006710397.3:c.2275C>A (DPYD)	XP_006710460.1:p.Arg759=
XM_017000507.1:c.2164C>A (DPYD)	XP_016855996.1:p.Arg722=
XM_017000508.2:c.1780C>A (DPYD)	XP_016855997.1:p.Arg594=
XM_017000509.2:c.1780C>A (DPYD)	XP_016855998.1:p.Arg594=
XM_017000510.1:c.1780C>A (DPYD)	XP_016855999.1:p.Arg594=
NM_000110.4:c.2275C>A (DPYD) MANE Select	NP_000101.2:p.Arg759=