Canonical Allele Identifier: CA1182843743

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97382415G= , CM000663.2:g.97382415G=	GRCh38
NC_000001.10:g.97847971G= , CM000663.1:g.97847971G=	GRCh37
NC_000001.9:g.97620559G=	NCBI36
NG_008807.2:g.543645C= , LRG_722:g.543645C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1952C= MANE Select	ENSP00000359211.3:p.Thr651=
ENST00000370192.7:c.1952C=	ENSP00000359211.3:p.Thr651=
NM_000110.3:c.1952C= , LRG_722t1:c.1952C=	NP_000101.2:p.Thr651=
XM_005270562.3:c.1736C=	XP_005270619.2:p.Thr579=
XM_006710397.2:c.1952C=	XP_006710460.1:p.Thr651=
XR_947619.1:n.1347-1219G=
XR_947620.1:n.1125-1219G=
XR_947621.1:n.1347-1219G=
XM_006710397.3:c.1952C=	XP_006710460.1:p.Thr651=
XM_017000507.1:c.1841C=	XP_016855996.1:p.Thr614=
XM_017000508.2:c.1457C=	XP_016855997.1:p.Thr486=
XM_017000509.2:c.1457C=	XP_016855998.1:p.Thr486=
XM_017000510.1:c.1457C=	XP_016855999.1:p.Thr486=
XR_001737686.2:n.692-1219G=
XR_001737687.1:n.692-1219G=
XR_001737688.2:n.692-1219G=
NM_000110.4:c.1952C= MANE Select	NP_000101.2:p.Thr651=