Canonical Allele Identifier: CA1183039451

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97828189T= , CM000663.2:g.97828189T=	GRCh38
NC_000001.10:g.98293745T= , CM000663.1:g.98293745T=	GRCh37
NC_000001.9:g.98066333T=	NCBI36
NG_008807.2:g.97871A= , LRG_722:g.97871A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.158A= MANE Select	ENSP00000359211.3:p.Glu53=
ENST00000306031.5:c.158A=	ENSP00000307107.5:p.Glu53=
ENST00000370192.7:c.158A=	ENSP00000359211.3:p.Glu53=
NM_000110.3:c.158A= , LRG_722t1:c.158A=	NP_000101.2:p.Glu53=
NM_001160301.1:c.158A= , LRG_722t2:c.158A=	NP_001153773.1:p.Glu53=
XM_005270562.3:c.158A=	XP_005270619.2:p.Glu53=
XM_006710397.2:c.158A=	XP_006710460.1:p.Glu53=
XM_006710397.3:c.158A=	XP_006710460.1:p.Glu53=
XM_017000507.1:c.47A=	XP_016855996.1:p.Glu16=
XM_017000508.2:c.-553A=	XP_016855997.1:n.-553A=
XM_017000509.2:c.-451A=	XP_016855998.1:n.-451A=
XM_017000510.1:c.-451A=	XP_016855999.1:n.-451A=
XR_001737014.1:n.295A=
NM_000110.4:c.158A= MANE Select	NP_000101.2:p.Glu53=