Canonical Allele Identifier: CA1183039436

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97828138C= , CM000663.2:g.97828138C=	GRCh38
NC_000001.10:g.98293694C= , CM000663.1:g.98293694C=	GRCh37
NC_000001.9:g.98066282C=	NCBI36
NG_008807.2:g.97922G= , LRG_722:g.97922G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.209G= MANE Select	ENSP00000359211.3:p.Arg70=
ENST00000306031.5:c.209G=	ENSP00000307107.5:p.Arg70=
ENST00000370192.7:c.209G=	ENSP00000359211.3:p.Arg70=
NM_000110.3:c.209G= , LRG_722t1:c.209G=	NP_000101.2:p.Arg70=
NM_001160301.1:c.209G= , LRG_722t2:c.209G=	NP_001153773.1:p.Arg70=
XM_005270562.3:c.209G=	XP_005270619.2:p.Arg70=
XM_006710397.2:c.209G=	XP_006710460.1:p.Arg70=
XM_006710397.3:c.209G=	XP_006710460.1:p.Arg70=
XM_017000507.1:c.98G=	XP_016855996.1:p.Arg33=
XM_017000508.2:c.-502G=	XP_016855997.1:n.-502G=
XM_017000509.2:c.-400G=	XP_016855998.1:n.-400G=
XM_017000510.1:c.-400G=	XP_016855999.1:n.-400G=
XR_001737014.1:n.346G=
NM_000110.4:c.209G= MANE Select	NP_000101.2:p.Arg70=