Canonical Allele Identifier: CA1182917409

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97549619T= , CM000663.2:g.97549619T=	GRCh38
NC_000001.10:g.98015175T= , CM000663.1:g.98015175T=	GRCh37
NC_000001.9:g.97787763T=	NCBI36
NG_008807.2:g.376441A= , LRG_722:g.376441A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.1465A= MANE Select	ENSP00000359211.3:p.Thr489=
ENST00000370192.7:c.1465A=	ENSP00000359211.3:p.Thr489=
NM_000110.3:c.1465A= , LRG_722t1:c.1465A=	NP_000101.2:p.Thr489=
XM_005270562.3:c.1465A=	XP_005270619.2:p.Thr489=
XM_006710397.2:c.1465A=	XP_006710460.1:p.Thr489=
XM_006710397.3:c.1465A=	XP_006710460.1:p.Thr489=
XM_017000507.1:c.1354A=	XP_016855996.1:p.Thr452=
XM_017000508.2:c.970A=	XP_016855997.1:p.Thr324=
XM_017000509.2:c.970A=	XP_016855998.1:p.Thr324=
XM_017000510.1:c.970A=	XP_016855999.1:p.Thr324=
NM_000110.4:c.1465A= MANE Select	NP_000101.2:p.Thr489=