Canonical Allele Identifier: CA963050

Gene: DPYD DPYD-AS1

Linked Data

• dbSNP Id: rs758649719
• ExAC: 1:97700491 C / T
• gnomAD v2: 1-97700491-C-T
• gnomAD v4: 1-97234935-C-T
• MyVariant Identifiers: chr1:g.97700491C>T (hg19) ; chr1:g.97234935C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97234935C>T , CM000663.2:g.97234935C>T	GRCh38
NC_000001.10:g.97700491C>T , CM000663.1:g.97700491C>T	GRCh37
NC_000001.9:g.97473079C>T	NCBI36
NG_008807.2:g.691125G>A , LRG_722:g.691125G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2359G>A (DPYD) MANE Select	ENSP00000359211.3:p.Gly787Arg
ENST00000370192.7:c.2359G>A (DPYD)	ENSP00000359211.3:p.Gly787Arg
NM_000110.3:c.2359G>A , LRG_722t1:c.2359G>A (DPYD)	NP_000101.2:p.Gly787Arg
NR_046590.1:n.65-30479C>T (DPYD-AS1)
XM_005270562.3:c.2143G>A (DPYD)	XP_005270619.2:p.Gly715Arg
XM_006710397.2:c.2359G>A (DPYD)	XP_006710460.1:p.Gly787Arg
XM_006710397.3:c.2359G>A (DPYD)	XP_006710460.1:p.Gly787Arg
XM_017000507.1:c.2248G>A (DPYD)	XP_016855996.1:p.Gly750Arg
XM_017000508.2:c.1864G>A (DPYD)	XP_016855997.1:p.Gly622Arg
XM_017000509.2:c.1864G>A (DPYD)	XP_016855998.1:p.Gly622Arg
XM_017000510.1:c.1864G>A (DPYD)	XP_016855999.1:p.Gly622Arg
NM_000110.4:c.2359G>A (DPYD) MANE Select	NP_000101.2:p.Gly787Arg