Canonical Allele Identifier: CA1182832713

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97357228T= , CM000663.2:g.97357228T=	GRCh38
NC_000001.10:g.97822784T= , CM000663.1:g.97822784T=	GRCh37
NC_000001.9:g.97595372T=	NCBI36
NG_008807.2:g.568832A= , LRG_722:g.568832A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2058+16333A= MANE Select	ENSP00000359211.3:n.2058+16333A=
ENST00000370192.7:c.2058+16333A=	ENSP00000359211.3:n.2058+16333A=
NM_000110.3:c.2058+16333A= , LRG_722t1:c.2058+16333A=	NP_000101.2:n.2058+16333A=
XM_005270562.3:c.1842+16333A=	XP_005270619.2:n.1842+16333A=
XM_006710397.2:c.2058+16333A=	XP_006710460.1:n.2058+16333A=
XR_947619.1:n.921-9770T=
XR_947620.1:n.921-9770T=
XR_947621.1:n.921-9770T=
XM_006710397.3:c.2058+16333A=	XP_006710460.1:n.2058+16333A=
XM_017000507.1:c.1947+16333A=	XP_016855996.1:n.1947+16333A=
XM_017000508.2:c.1563+16333A=	XP_016855997.1:n.1563+16333A=
XM_017000509.2:c.1563+16333A=	XP_016855998.1:n.1563+16333A=
XM_017000510.1:c.1563+16333A=	XP_016855999.1:n.1563+16333A=
NM_000110.4:c.2058+16333A= MANE Select	NP_000101.2:n.2058+16333A=