Canonical Allele Identifier: CA1143359197

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97549681G= , CM000663.2:g.97549681G=	GRCh38
NC_000001.10:g.98015237G= , CM000663.1:g.98015237G=	GRCh37
NC_000001.9:g.97787825G=	NCBI36
NG_008807.2:g.376379C= , LRG_722:g.376379C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1403C= MANE Select	ENSP00000359211.3:p.Thr468=
ENST00000370192.7:c.1403C=	ENSP00000359211.3:p.Thr468=
NM_000110.3:c.1403C= , LRG_722t1:c.1403C=	NP_000101.2:p.Thr468=
XM_005270562.3:c.1403C=	XP_005270619.2:p.Thr468=
XM_006710397.2:c.1403C=	XP_006710460.1:p.Thr468=
XM_006710397.3:c.1403C=	XP_006710460.1:p.Thr468=
XM_017000507.1:c.1292C=	XP_016855996.1:p.Thr431=
XM_017000508.2:c.908C=	XP_016855997.1:p.Thr303=
XM_017000509.2:c.908C=	XP_016855998.1:p.Thr303=
XM_017000510.1:c.908C=	XP_016855999.1:p.Thr303=
NM_000110.4:c.1403C= MANE Select	NP_000101.2:p.Thr468=