Canonical Allele Identifier: CA341375230

Gene: DPYD DPYD-AS1

Linked Data

• dbSNP Id: rs1262788717
• MyVariant Identifiers: chr1:g.97770925T>G (hg19) ; chr1:g.97305369T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97305369T>G , CM000663.2:g.97305369T>G	GRCh38
NC_000001.10:g.97770925T>G , CM000663.1:g.97770925T>G	GRCh37
NC_000001.9:g.97543513T>G	NCBI36
NG_008807.2:g.620691A>C , LRG_722:g.620691A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.2189A>C (DPYD) MANE Select	ENSP00000359211.3:p.Asn730Thr
ENST00000370192.7:c.2189A>C (DPYD)	ENSP00000359211.3:p.Asn730Thr
NM_000110.3:c.2189A>C , LRG_722t1:c.2189A>C (DPYD)	NP_000101.2:p.Asn730Thr
NR_046590.1:n.129-820T>G (DPYD-AS1)
XM_005270562.3:c.1973A>C (DPYD)	XP_005270619.2:p.Asn658Thr
XM_006710397.2:c.2189A>C (DPYD)	XP_006710460.1:p.Asn730Thr
XM_006710397.3:c.2189A>C (DPYD)	XP_006710460.1:p.Asn730Thr
XM_017000507.1:c.2078A>C (DPYD)	XP_016855996.1:p.Asn693Thr
XM_017000508.2:c.1694A>C (DPYD)	XP_016855997.1:p.Asn565Thr
XM_017000509.2:c.1694A>C (DPYD)	XP_016855998.1:p.Asn565Thr
XM_017000510.1:c.1694A>C (DPYD)	XP_016855999.1:p.Asn565Thr
NM_000110.4:c.2189A>C (DPYD) MANE Select	NP_000101.2:p.Asn730Thr