Canonical Allele Identifier: CA341375037

Gene: DPYD DPYD-AS1

Linked Data

• dbSNP Id: rs2101035625
• MyVariant Identifiers: chr1:g.97770830A>T (hg19) ; chr1:g.97305274A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97305274A>T , CM000663.2:g.97305274A>T	GRCh38
NC_000001.10:g.97770830A>T , CM000663.1:g.97770830A>T	GRCh37
NC_000001.9:g.97543418A>T	NCBI36
NG_008807.2:g.620786T>A , LRG_722:g.620786T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.2284T>A (DPYD) MANE Select	ENSP00000359211.3:p.Tyr762Asn
ENST00000370192.7:c.2284T>A (DPYD)	ENSP00000359211.3:p.Tyr762Asn
NM_000110.3:c.2284T>A , LRG_722t1:c.2284T>A (DPYD)	NP_000101.2:p.Tyr762Asn
NR_046590.1:n.129-915A>T (DPYD-AS1)
XM_005270562.3:c.2068T>A (DPYD)	XP_005270619.2:p.Tyr690Asn
XM_006710397.2:c.2284T>A (DPYD)	XP_006710460.1:p.Tyr762Asn
XM_006710397.3:c.2284T>A (DPYD)	XP_006710460.1:p.Tyr762Asn
XM_017000507.1:c.2173T>A (DPYD)	XP_016855996.1:p.Tyr725Asn
XM_017000508.2:c.1789T>A (DPYD)	XP_016855997.1:p.Tyr597Asn
XM_017000509.2:c.1789T>A (DPYD)	XP_016855998.1:p.Tyr597Asn
XM_017000510.1:c.1789T>A (DPYD)	XP_016855999.1:p.Tyr597Asn
NM_000110.4:c.2284T>A (DPYD) MANE Select	NP_000101.2:p.Tyr762Asn