Canonical Allele Identifier: CA1182717189

Gene: DPYD DPYD-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97098516G= , CM000663.2:g.97098516G=	GRCh38
NC_000001.10:g.97564072G= , CM000663.1:g.97564072G=	GRCh37
NC_000001.9:g.97336660G=	NCBI36
NG_008807.2:g.827544C= , LRG_722:g.827544C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.2739C= (DPYD) MANE Select	ENSP00000359211.3:p.Ile913=
ENST00000370192.7:c.2739C= (DPYD)	ENSP00000359211.3:p.Ile913=
NM_000110.3:c.2739C= , LRG_722t1:c.2739C= (DPYD)	NP_000101.2:p.Ile913=
NR_046590.1:n.64+2530G= (DPYD-AS1)
XM_005270562.3:c.2523C= (DPYD)	XP_005270619.2:p.Ile841=
XM_017000507.1:c.2628C= (DPYD)	XP_016855996.1:p.Ile876=
XM_017000508.2:c.2244C= (DPYD)	XP_016855997.1:p.Ile748=
XM_017000509.2:c.2244C= (DPYD)	XP_016855998.1:p.Ile748=
XM_017000510.1:c.2244C= (DPYD)	XP_016855999.1:p.Ile748=
NM_000110.4:c.2739C= (DPYD) MANE Select	NP_000101.2:p.Ile913=