Canonical Allele Identifier: CA1142099116

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97699370C= , CM000663.2:g.97699370C=	GRCh38
NC_000001.10:g.98164926C= , CM000663.1:g.98164926C=	GRCh37
NC_000001.9:g.97937514C=	NCBI36
NG_008807.2:g.226690G= , LRG_722:g.226690G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.661G= MANE Select	ENSP00000359211.3:p.Glu221=
ENST00000370192.7:c.661G=	ENSP00000359211.3:p.Glu221=
ENST00000474241.1:n.425G=
NM_000110.3:c.661G= , LRG_722t1:c.661G=	NP_000101.2:p.Glu221=
XM_005270562.3:c.661G=	XP_005270619.2:p.Glu221=
XM_006710397.2:c.661G=	XP_006710460.1:p.Glu221=
XM_006710397.3:c.661G=	XP_006710460.1:p.Glu221=
XM_017000507.1:c.550G=	XP_016855996.1:p.Glu184=
XM_017000508.2:c.166G=	XP_016855997.1:p.Glu56=
XM_017000509.2:c.166G=	XP_016855998.1:p.Glu56=
XM_017000510.1:c.166G=	XP_016855999.1:p.Glu56=
NM_000110.4:c.661G= MANE Select	NP_000101.2:p.Glu221=