Canonical Allele Identifier: CA341375238

Gene: DPYD DPYD-AS1

Linked Data

• ClinVar Variation Id: 1805513
• ClinVar RCV Id: RCV002471931
• dbSNP Id: rs2101036846
• MyVariant Identifiers: chr1:g.97770931C>A (hg19) ; chr1:g.97305375C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97305375C>A , CM000663.2:g.97305375C>A	GRCh38
NC_000001.10:g.97770931C>A , CM000663.1:g.97770931C>A	GRCh37
NC_000001.9:g.97543519C>A	NCBI36
NG_008807.2:g.620685G>T , LRG_722:g.620685G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.2183G>T (DPYD) MANE Select	ENSP00000359211.3:p.Gly728Val
ENST00000370192.7:c.2183G>T (DPYD)	ENSP00000359211.3:p.Gly728Val
NM_000110.3:c.2183G>T , LRG_722t1:c.2183G>T (DPYD)	NP_000101.2:p.Gly728Val
NR_046590.1:n.129-814C>A (DPYD-AS1)
XM_005270562.3:c.1967G>T (DPYD)	XP_005270619.2:p.Gly656Val
XM_006710397.2:c.2183G>T (DPYD)	XP_006710460.1:p.Gly728Val
XM_006710397.3:c.2183G>T (DPYD)	XP_006710460.1:p.Gly728Val
XM_017000507.1:c.2072G>T (DPYD)	XP_016855996.1:p.Gly691Val
XM_017000508.2:c.1688G>T (DPYD)	XP_016855997.1:p.Gly563Val
XM_017000509.2:c.1688G>T (DPYD)	XP_016855998.1:p.Gly563Val
XM_017000510.1:c.1688G>T (DPYD)	XP_016855999.1:p.Gly563Val
NM_000110.4:c.2183G>T (DPYD) MANE Select	NP_000101.2:p.Gly728Val