Canonical Allele Identifier: CA341374858

Gene: DPYD DPYD-AS1

Linked Data

• MyVariant Identifiers: chr1:g.97564124C>G (hg19) ; chr1:g.97098568C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97098568C>G , CM000663.2:g.97098568C>G	GRCh38
NC_000001.10:g.97564124C>G , CM000663.1:g.97564124C>G	GRCh37
NC_000001.9:g.97336712C>G	NCBI36
NG_008807.2:g.827492G>C , LRG_722:g.827492G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2687G>C (DPYD) MANE Select	ENSP00000359211.3:p.Arg896Thr
ENST00000370192.7:c.2687G>C (DPYD)	ENSP00000359211.3:p.Arg896Thr
NM_000110.3:c.2687G>C , LRG_722t1:c.2687G>C (DPYD)	NP_000101.2:p.Arg896Thr
NR_046590.1:n.64+2582C>G (DPYD-AS1)
XM_005270562.3:c.2471G>C (DPYD)	XP_005270619.2:p.Arg824Thr
XM_017000507.1:c.2576G>C (DPYD)	XP_016855996.1:p.Arg859Thr
XM_017000508.2:c.2192G>C (DPYD)	XP_016855997.1:p.Arg731Thr
XM_017000509.2:c.2192G>C (DPYD)	XP_016855998.1:p.Arg731Thr
XM_017000510.1:c.2192G>C (DPYD)	XP_016855999.1:p.Arg731Thr
NM_000110.4:c.2687G>C (DPYD) MANE Select	NP_000101.2:p.Arg896Thr