Canonical Allele Identifier: CA1143408435

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97450063T= , CM000663.2:g.97450063T=	GRCh38
NC_000001.10:g.97915619T= , CM000663.1:g.97915619T=	GRCh37
NC_000001.9:g.97688207T=	NCBI36
NG_008807.2:g.475997A= , LRG_722:g.475997A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1901A= MANE Select	ENSP00000359211.3:p.Asp634=
ENST00000370192.7:c.1901A=	ENSP00000359211.3:p.Asp634=
NM_000110.3:c.1901A= , LRG_722t1:c.1901A=	NP_000101.2:p.Asp634=
XM_005270562.3:c.1685A=	XP_005270619.2:p.Asp562=
XM_006710397.2:c.1901A=	XP_006710460.1:p.Asp634=
XM_006710397.3:c.1901A=	XP_006710460.1:p.Asp634=
XM_017000507.1:c.1790A=	XP_016855996.1:p.Asp597=
XM_017000508.2:c.1406A=	XP_016855997.1:p.Asp469=
XM_017000509.2:c.1406A=	XP_016855998.1:p.Asp469=
XM_017000510.1:c.1406A=	XP_016855999.1:p.Asp469=
NM_000110.4:c.1901A= MANE Select	NP_000101.2:p.Asp634=