Canonical Allele Identifier: CA341373396

Gene: DPYD DPYD-AS1

Linked Data

• dbSNP Id: rs1331845069
• MyVariant Identifiers: chr1:g.97658687G>C (hg19) ; chr1:g.97193131G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97193131G>C , CM000663.2:g.97193131G>C	GRCh38
NC_000001.10:g.97658687G>C , CM000663.1:g.97658687G>C	GRCh37
NC_000001.9:g.97431275G>C	NCBI36
NG_008807.2:g.732929C>G , LRG_722:g.732929C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2560C>G (DPYD) MANE Select	ENSP00000359211.3:p.Pro854Ala
ENST00000370192.7:c.2560C>G (DPYD)	ENSP00000359211.3:p.Pro854Ala
NM_000110.3:c.2560C>G , LRG_722t1:c.2560C>G (DPYD)	NP_000101.2:p.Pro854Ala
NR_046590.1:n.65-72283G>C (DPYD-AS1)
XM_005270562.3:c.2344C>G (DPYD)	XP_005270619.2:p.Pro782Ala
XM_006710397.2:c.2560C>G (DPYD)	XP_006710460.1:p.Pro854Ala
XM_006710397.3:c.2560C>G (DPYD)	XP_006710460.1:p.Pro854Ala
XM_017000507.1:c.2449C>G (DPYD)	XP_016855996.1:p.Pro817Ala
XM_017000508.2:c.2065C>G (DPYD)	XP_016855997.1:p.Pro689Ala
XM_017000509.2:c.2065C>G (DPYD)	XP_016855998.1:p.Pro689Ala
XM_017000510.1:c.2065C>G (DPYD)	XP_016855999.1:p.Pro689Ala
NM_000110.4:c.2560C>G (DPYD) MANE Select	NP_000101.2:p.Pro854Ala