Canonical Allele Identifier: CA419137427

Gene: DPYD DPYD-AS1

Linked Data

• MyVariant Identifiers: chr1:g.97770846A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97305290A>T , CM000663.2:g.97305290A>T	GRCh38
NC_000001.10:g.97770846A>T , CM000663.1:g.97770846A>T	GRCh37
NC_000001.9:g.97543434A>T	NCBI36
NG_008807.2:g.620770T>A , LRG_722:g.620770T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2268T>A (DPYD) MANE Select	ENSP00000359211.3:p.Ile756=
ENST00000370192.7:c.2268T>A (DPYD)	ENSP00000359211.3:p.Ile756=
NM_000110.3:c.2268T>A , LRG_722t1:c.2268T>A (DPYD)	NP_000101.2:p.Ile756=
NR_046590.1:n.129-899A>T (DPYD-AS1)
XM_005270562.3:c.2052T>A (DPYD)	XP_005270619.2:p.Ile684=
XM_006710397.2:c.2268T>A (DPYD)	XP_006710460.1:p.Ile756=
XM_006710397.3:c.2268T>A (DPYD)	XP_006710460.1:p.Ile756=
XM_017000507.1:c.2157T>A (DPYD)	XP_016855996.1:p.Ile719=
XM_017000508.2:c.1773T>A (DPYD)	XP_016855997.1:p.Ile591=
XM_017000509.2:c.1773T>A (DPYD)	XP_016855998.1:p.Ile591=
XM_017000510.1:c.1773T>A (DPYD)	XP_016855999.1:p.Ile591=
NM_000110.4:c.2268T>A (DPYD) MANE Select	NP_000101.2:p.Ile756=