Canonical Allele Identifier: CA419137482

Gene: DPYD DPYD-AS1

Linked Data

• MyVariant Identifiers: chr1:g.97770915T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97305359T>G , CM000663.2:g.97305359T>G	GRCh38
NC_000001.10:g.97770915T>G , CM000663.1:g.97770915T>G	GRCh37
NC_000001.9:g.97543503T>G	NCBI36
NG_008807.2:g.620701A>C , LRG_722:g.620701A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2199A>C (DPYD) MANE Select	ENSP00000359211.3:p.Thr733=
ENST00000370192.7:c.2199A>C (DPYD)	ENSP00000359211.3:p.Thr733=
NM_000110.3:c.2199A>C , LRG_722t1:c.2199A>C (DPYD)	NP_000101.2:p.Thr733=
NR_046590.1:n.129-830T>G (DPYD-AS1)
XM_005270562.3:c.1983A>C (DPYD)	XP_005270619.2:p.Thr661=
XM_006710397.2:c.2199A>C (DPYD)	XP_006710460.1:p.Thr733=
XM_006710397.3:c.2199A>C (DPYD)	XP_006710460.1:p.Thr733=
XM_017000507.1:c.2088A>C (DPYD)	XP_016855996.1:p.Thr696=
XM_017000508.2:c.1704A>C (DPYD)	XP_016855997.1:p.Thr568=
XM_017000509.2:c.1704A>C (DPYD)	XP_016855998.1:p.Thr568=
XM_017000510.1:c.1704A>C (DPYD)	XP_016855999.1:p.Thr568=
NM_000110.4:c.2199A>C (DPYD) MANE Select	NP_000101.2:p.Thr733=