Canonical Allele Identifier: CA1182843742

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97382413C= , CM000663.2:g.97382413C=	GRCh38
NC_000001.10:g.97847969C= , CM000663.1:g.97847969C=	GRCh37
NC_000001.9:g.97620557C=	NCBI36
NG_008807.2:g.543647G= , LRG_722:g.543647G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1954G= MANE Select	ENSP00000359211.3:p.Glu652=
ENST00000370192.7:c.1954G=	ENSP00000359211.3:p.Glu652=
NM_000110.3:c.1954G= , LRG_722t1:c.1954G=	NP_000101.2:p.Glu652=
XM_005270562.3:c.1738G=	XP_005270619.2:p.Glu580=
XM_006710397.2:c.1954G=	XP_006710460.1:p.Glu652=
XR_947619.1:n.1347-1221C=
XR_947620.1:n.1125-1221C=
XR_947621.1:n.1347-1221C=
XM_006710397.3:c.1954G=	XP_006710460.1:p.Glu652=
XM_017000507.1:c.1843G=	XP_016855996.1:p.Glu615=
XM_017000508.2:c.1459G=	XP_016855997.1:p.Glu487=
XM_017000509.2:c.1459G=	XP_016855998.1:p.Glu487=
XM_017000510.1:c.1459G=	XP_016855999.1:p.Glu487=
XR_001737686.2:n.692-1221C=
XR_001737687.1:n.692-1221C=
XR_001737688.2:n.692-1221C=
NM_000110.4:c.1954G= MANE Select	NP_000101.2:p.Glu652=