Canonical Allele Identifier: CA1182776929

Gene: DPYD DPYD-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97234915A= , CM000663.2:g.97234915A=	GRCh38
NC_000001.10:g.97700471A= , CM000663.1:g.97700471A=	GRCh37
NC_000001.9:g.97473059A=	NCBI36
NG_008807.2:g.691145T= , LRG_722:g.691145T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2379T= (DPYD) MANE Select	ENSP00000359211.3:p.Thr793=
ENST00000370192.7:c.2379T= (DPYD)	ENSP00000359211.3:p.Thr793=
NM_000110.3:c.2379T= , LRG_722t1:c.2379T= (DPYD)	NP_000101.2:p.Thr793=
NR_046590.1:n.65-30499A= (DPYD-AS1)
XM_005270562.3:c.2163T= (DPYD)	XP_005270619.2:p.Thr721=
XM_006710397.2:c.2379T= (DPYD)	XP_006710460.1:p.Thr793=
XM_006710397.3:c.2379T= (DPYD)	XP_006710460.1:p.Thr793=
XM_017000507.1:c.2268T= (DPYD)	XP_016855996.1:p.Thr756=
XM_017000508.2:c.1884T= (DPYD)	XP_016855997.1:p.Thr628=
XM_017000509.2:c.1884T= (DPYD)	XP_016855998.1:p.Thr628=
XM_017000510.1:c.1884T= (DPYD)	XP_016855999.1:p.Thr628=
NM_000110.4:c.2379T= (DPYD) MANE Select	NP_000101.2:p.Thr793=