Canonical Allele Identifier: CA341373643

Gene: DPYD DPYD-AS1

Linked Data

• gnomAD v4: 1-97193241-C-A
• MyVariant Identifiers: chr1:g.97658797C>A (hg19) ; chr1:g.97193241C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97193241C>A , CM000663.2:g.97193241C>A	GRCh38
NC_000001.10:g.97658797C>A , CM000663.1:g.97658797C>A	GRCh37
NC_000001.9:g.97431385C>A	NCBI36
NG_008807.2:g.732819G>T , LRG_722:g.732819G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2450G>T (DPYD) MANE Select	ENSP00000359211.3:p.Ser817Ile
ENST00000370192.7:c.2450G>T (DPYD)	ENSP00000359211.3:p.Ser817Ile
NM_000110.3:c.2450G>T , LRG_722t1:c.2450G>T (DPYD)	NP_000101.2:p.Ser817Ile
NR_046590.1:n.65-72173C>A (DPYD-AS1)
XM_005270562.3:c.2234G>T (DPYD)	XP_005270619.2:p.Ser745Ile
XM_006710397.2:c.2450G>T (DPYD)	XP_006710460.1:p.Ser817Ile
XM_006710397.3:c.2450G>T (DPYD)	XP_006710460.1:p.Ser817Ile
XM_017000507.1:c.2339G>T (DPYD)	XP_016855996.1:p.Ser780Ile
XM_017000508.2:c.1955G>T (DPYD)	XP_016855997.1:p.Ser652Ile
XM_017000509.2:c.1955G>T (DPYD)	XP_016855998.1:p.Ser652Ile
XM_017000510.1:c.1955G>T (DPYD)	XP_016855999.1:p.Ser652Ile
NM_000110.4:c.2450G>T (DPYD) MANE Select	NP_000101.2:p.Ser817Ile