Canonical Allele Identifier: CA1183039433

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97828129A= , CM000663.2:g.97828129A=	GRCh38
NC_000001.10:g.98293685A= , CM000663.1:g.98293685A=	GRCh37
NC_000001.9:g.98066273A=	NCBI36
NG_008807.2:g.97931T= , LRG_722:g.97931T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.218T= MANE Select	ENSP00000359211.3:p.Leu73=
ENST00000306031.5:c.218T=	ENSP00000307107.5:p.Leu73=
ENST00000370192.7:c.218T=	ENSP00000359211.3:p.Leu73=
NM_000110.3:c.218T= , LRG_722t1:c.218T=	NP_000101.2:p.Leu73=
NM_001160301.1:c.218T= , LRG_722t2:c.218T=	NP_001153773.1:p.Leu73=
XM_005270562.3:c.218T=	XP_005270619.2:p.Leu73=
XM_006710397.2:c.218T=	XP_006710460.1:p.Leu73=
XM_006710397.3:c.218T=	XP_006710460.1:p.Leu73=
XM_017000507.1:c.107T=	XP_016855996.1:p.Leu36=
XM_017000508.2:c.-493T=	XP_016855997.1:n.-493T=
XM_017000509.2:c.-391T=	XP_016855998.1:n.-391T=
XM_017000510.1:c.-391T=	XP_016855999.1:n.-391T=
XR_001737014.1:n.355T=
NM_000110.4:c.218T= MANE Select	NP_000101.2:p.Leu73=