Canonical Allele Identifier: CA1141452999

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97699474T= , CM000663.2:g.97699474T=	GRCh38
NC_000001.10:g.98165030T= , CM000663.1:g.98165030T=	GRCh37
NC_000001.9:g.97937618T=	NCBI36
NG_008807.2:g.226586A= , LRG_722:g.226586A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000110.4:c.557A= MANE Select	NP_000101.2:p.Tyr186=
ENST00000370192.8:c.557A= MANE Select	ENSP00000359211.3:p.Tyr186=
NM_000110.3:c.557A= , LRG_722t1:c.557A=	NP_000101.2:p.Tyr186=
ENST00000370192.7:c.557A=	ENSP00000359211.3:p.Tyr186=
ENST00000474241.1:n.321A=
XM_005270562.3:c.557A=	XP_005270619.2:p.Tyr186=
XM_006710397.2:c.557A=	XP_006710460.1:p.Tyr186=
XM_006710397.3:c.557A=	XP_006710460.1:p.Tyr186=
XM_017000507.1:c.446A=	XP_016855996.1:p.Tyr149=
XM_017000508.2:c.62A=	XP_016855997.1:p.Tyr21=
XM_017000509.2:c.62A=	XP_016855998.1:p.Tyr21=
XM_017000510.1:c.62A=	XP_016855999.1:p.Tyr21=