Canonical Allele Identifier: CA1182878149

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97461188C= , CM000663.2:g.97461188C=	GRCh38
NC_000001.10:g.97926744C= , CM000663.1:g.97926744C=	GRCh37
NC_000001.9:g.97699332C=	NCBI36
NG_008807.2:g.464872G= , LRG_722:g.464872G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1741-10965G= MANE Select	ENSP00000359211.3:n.1741-10965G=
ENST00000370192.7:c.1741-10965G=	ENSP00000359211.3:n.1741-10965G=
NM_000110.3:c.1741-10965G= , LRG_722t1:c.1741-10965G=	NP_000101.2:n.1741-10965G=
XM_005270562.3:c.1525-10965G=	XP_005270619.2:n.1525-10965G=
XM_006710397.2:c.1741-10965G=	XP_006710460.1:n.1741-10965G=
XM_006710397.3:c.1741-10965G=	XP_006710460.1:n.1741-10965G=
XM_017000507.1:c.1630-10965G=	XP_016855996.1:n.1630-10965G=
XM_017000508.2:c.1246-10965G=	XP_016855997.1:n.1246-10965G=
XM_017000509.2:c.1246-10965G=	XP_016855998.1:n.1246-10965G=
XM_017000510.1:c.1246-10965G=	XP_016855999.1:n.1246-10965G=
NM_000110.4:c.1741-10965G= MANE Select	NP_000101.2:n.1741-10965G=