Canonical Allele Identifier: CA341373385

Gene: DPYD DPYD-AS1

Linked Data

• MyVariant Identifiers: chr1:g.97658681T>G (hg19) ; chr1:g.97193125T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97193125T>G , CM000663.2:g.97193125T>G	GRCh38
NC_000001.10:g.97658681T>G , CM000663.1:g.97658681T>G	GRCh37
NC_000001.9:g.97431269T>G	NCBI36
NG_008807.2:g.732935A>C , LRG_722:g.732935A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2566A>C (DPYD) MANE Select	ENSP00000359211.3:p.Thr856Pro
ENST00000370192.7:c.2566A>C (DPYD)	ENSP00000359211.3:p.Thr856Pro
NM_000110.3:c.2566A>C , LRG_722t1:c.2566A>C (DPYD)	NP_000101.2:p.Thr856Pro
NR_046590.1:n.65-72289T>G (DPYD-AS1)
XM_005270562.3:c.2350A>C (DPYD)	XP_005270619.2:p.Thr784Pro
XM_006710397.2:c.2566A>C (DPYD)	XP_006710460.1:p.Thr856Pro
XM_006710397.3:c.2566A>C (DPYD)	XP_006710460.1:p.Thr856Pro
XM_017000507.1:c.2455A>C (DPYD)	XP_016855996.1:p.Thr819Pro
XM_017000508.2:c.2071A>C (DPYD)	XP_016855997.1:p.Thr691Pro
XM_017000509.2:c.2071A>C (DPYD)	XP_016855998.1:p.Thr691Pro
XM_017000510.1:c.2071A>C (DPYD)	XP_016855999.1:p.Thr691Pro
NM_000110.4:c.2566A>C (DPYD) MANE Select	NP_000101.2:p.Thr856Pro