Canonical Allele Identifier: CA2574442146

Gene: DPYD DPYD-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97305352_97305356dup , CM000663.2:g.97305352_97305356dup	GRCh38
NC_000001.10:g.97770908_97770912dup , CM000663.1:g.97770908_97770912dup	GRCh37
NC_000001.9:g.97543496_97543500dup	NCBI36
NG_008807.2:g.620704_620708dup , LRG_722:g.620704_620708dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2202_2206dup (DPYD) MANE Select	ENSP00000359211.3:p.Asn736ThrfsTer8
ENST00000370192.7:c.2202_2206dup (DPYD)	ENSP00000359211.3:p.Asn736ThrfsTer8
NM_000110.3:c.2202_2206dup , LRG_722t1:c.2202_2206dup (DPYD)	NP_000101.2:p.Asn736ThrfsTer8
NR_046590.1:n.129-837_129-833dup (DPYD-AS1)
XM_005270562.3:c.1986_1990dup (DPYD)	XP_005270619.2:p.Asn664ThrfsTer8
XM_006710397.2:c.2202_2206dup (DPYD)	XP_006710460.1:p.Asn736ThrfsTer8
XM_006710397.3:c.2202_2206dup (DPYD)	XP_006710460.1:p.Asn736ThrfsTer8
XM_017000507.1:c.2091_2095dup (DPYD)	XP_016855996.1:p.Asn699ThrfsTer8
XM_017000508.2:c.1707_1711dup (DPYD)	XP_016855997.1:p.Asn571ThrfsTer8
XM_017000509.2:c.1707_1711dup (DPYD)	XP_016855998.1:p.Asn571ThrfsTer8
XM_017000510.1:c.1707_1711dup (DPYD)	XP_016855999.1:p.Asn571ThrfsTer8
NM_000110.4:c.2202_2206dup (DPYD) MANE Select	NP_000101.2:p.Asn736ThrfsTer8