Canonical Allele Identifier: CA341375093

Gene: DPYD DPYD-AS1

Linked Data

• MyVariant Identifiers: chr1:g.97770860G>T (hg19) ; chr1:g.97305304G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97305304G>T , CM000663.2:g.97305304G>T	GRCh38
NC_000001.10:g.97770860G>T , CM000663.1:g.97770860G>T	GRCh37
NC_000001.9:g.97543448G>T	NCBI36
NG_008807.2:g.620756C>A , LRG_722:g.620756C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2254C>A (DPYD) MANE Select	ENSP00000359211.3:p.Pro752Thr
ENST00000370192.7:c.2254C>A (DPYD)	ENSP00000359211.3:p.Pro752Thr
NM_000110.3:c.2254C>A , LRG_722t1:c.2254C>A (DPYD)	NP_000101.2:p.Pro752Thr
NR_046590.1:n.129-885G>T (DPYD-AS1)
XM_005270562.3:c.2038C>A (DPYD)	XP_005270619.2:p.Pro680Thr
XM_006710397.2:c.2254C>A (DPYD)	XP_006710460.1:p.Pro752Thr
XM_006710397.3:c.2254C>A (DPYD)	XP_006710460.1:p.Pro752Thr
XM_017000507.1:c.2143C>A (DPYD)	XP_016855996.1:p.Pro715Thr
XM_017000508.2:c.1759C>A (DPYD)	XP_016855997.1:p.Pro587Thr
XM_017000509.2:c.1759C>A (DPYD)	XP_016855998.1:p.Pro587Thr
XM_017000510.1:c.1759C>A (DPYD)	XP_016855999.1:p.Pro587Thr
NM_000110.4:c.2254C>A (DPYD) MANE Select	NP_000101.2:p.Pro752Thr