Canonical Allele Identifier: CA1182878216

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97461373T= , CM000663.2:g.97461373T=	GRCh38
NC_000001.10:g.97926929T= , CM000663.1:g.97926929T=	GRCh37
NC_000001.9:g.97699517T=	NCBI36
NG_008807.2:g.464687A= , LRG_722:g.464687A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1741-11150A= MANE Select	ENSP00000359211.3:n.1741-11150A=
ENST00000370192.7:c.1741-11150A=	ENSP00000359211.3:n.1741-11150A=
NM_000110.3:c.1741-11150A= , LRG_722t1:c.1741-11150A=	NP_000101.2:n.1741-11150A=
XM_005270562.3:c.1525-11150A=	XP_005270619.2:n.1525-11150A=
XM_006710397.2:c.1741-11150A=	XP_006710460.1:n.1741-11150A=
XM_006710397.3:c.1741-11150A=	XP_006710460.1:n.1741-11150A=
XM_017000507.1:c.1630-11150A=	XP_016855996.1:n.1630-11150A=
XM_017000508.2:c.1246-11150A=	XP_016855997.1:n.1246-11150A=
XM_017000509.2:c.1246-11150A=	XP_016855998.1:n.1246-11150A=
XM_017000510.1:c.1246-11150A=	XP_016855999.1:n.1246-11150A=
NM_000110.4:c.1741-11150A= MANE Select	NP_000101.2:n.1741-11150A=