Canonical Allele Identifier: CA1141815175

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97828139G= , CM000663.2:g.97828139G=	GRCh38
NC_000001.10:g.98293695G= , CM000663.1:g.98293695G=	GRCh37
NC_000001.9:g.98066283G=	NCBI36
NG_008807.2:g.97921C= , LRG_722:g.97921C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.208C= MANE Select	ENSP00000359211.3:p.Arg70=
ENST00000306031.5:c.208C=	ENSP00000307107.5:p.Arg70=
ENST00000370192.7:c.208C=	ENSP00000359211.3:p.Arg70=
NM_000110.3:c.208C= , LRG_722t1:c.208C=	NP_000101.2:p.Arg70=
NM_001160301.1:c.208C= , LRG_722t2:c.208C=	NP_001153773.1:p.Arg70=
XM_005270562.3:c.208C=	XP_005270619.2:p.Arg70=
XM_006710397.2:c.208C=	XP_006710460.1:p.Arg70=
XM_006710397.3:c.208C=	XP_006710460.1:p.Arg70=
XM_017000507.1:c.97C=	XP_016855996.1:p.Arg33=
XM_017000508.2:c.-503C=	XP_016855997.1:n.-503C=
XM_017000509.2:c.-401C=	XP_016855998.1:n.-401C=
XM_017000510.1:c.-401C=	XP_016855999.1:n.-401C=
XR_001737014.1:n.345C=
NM_000110.4:c.208C= MANE Select	NP_000101.2:p.Arg70=