Canonical Allele Identifier: CA1182873449

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97450126A= , CM000663.2:g.97450126A=	GRCh38
NC_000001.10:g.97915682A= , CM000663.1:g.97915682A=	GRCh37
NC_000001.9:g.97688270A=	NCBI36
NG_008807.2:g.475934T= , LRG_722:g.475934T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.1838T= MANE Select	ENSP00000359211.3:p.Ile613=
ENST00000370192.7:c.1838T=	ENSP00000359211.3:p.Ile613=
NM_000110.3:c.1838T= , LRG_722t1:c.1838T=	NP_000101.2:p.Ile613=
XM_005270562.3:c.1622T=	XP_005270619.2:p.Ile541=
XM_006710397.2:c.1838T=	XP_006710460.1:p.Ile613=
XM_006710397.3:c.1838T=	XP_006710460.1:p.Ile613=
XM_017000507.1:c.1727T=	XP_016855996.1:p.Ile576=
XM_017000508.2:c.1343T=	XP_016855997.1:p.Ile448=
XM_017000509.2:c.1343T=	XP_016855998.1:p.Ile448=
XM_017000510.1:c.1343T=	XP_016855999.1:p.Ile448=
NM_000110.4:c.1838T= MANE Select	NP_000101.2:p.Ile613=