Canonical Allele Identifier: CA1182832754

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97357312G= , CM000663.2:g.97357312G=	GRCh38
NC_000001.10:g.97822868G= , CM000663.1:g.97822868G=	GRCh37
NC_000001.9:g.97595456G=	NCBI36
NG_008807.2:g.568748C= , LRG_722:g.568748C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2058+16249C= MANE Select	ENSP00000359211.3:n.2058+16249C=
ENST00000370192.7:c.2058+16249C=	ENSP00000359211.3:n.2058+16249C=
NM_000110.3:c.2058+16249C= , LRG_722t1:c.2058+16249C=	NP_000101.2:n.2058+16249C=
XM_005270562.3:c.1842+16249C=	XP_005270619.2:n.1842+16249C=
XM_006710397.2:c.2058+16249C=	XP_006710460.1:n.2058+16249C=
XR_947619.1:n.921-9686G=
XR_947620.1:n.921-9686G=
XR_947621.1:n.921-9686G=
XM_006710397.3:c.2058+16249C=	XP_006710460.1:n.2058+16249C=
XM_017000507.1:c.1947+16249C=	XP_016855996.1:n.1947+16249C=
XM_017000508.2:c.1563+16249C=	XP_016855997.1:n.1563+16249C=
XM_017000509.2:c.1563+16249C=	XP_016855998.1:n.1563+16249C=
XM_017000510.1:c.1563+16249C=	XP_016855999.1:n.1563+16249C=
NM_000110.4:c.2058+16249C= MANE Select	NP_000101.2:n.2058+16249C=