Canonical Allele Identifier: CA1182717194

Gene: DPYD DPYD-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97098532T= , CM000663.2:g.97098532T=	GRCh38
NC_000001.10:g.97564088T= , CM000663.1:g.97564088T=	GRCh37
NC_000001.9:g.97336676T=	NCBI36
NG_008807.2:g.827528A= , LRG_722:g.827528A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2723A= (DPYD) MANE Select	ENSP00000359211.3:p.Lys908=
ENST00000370192.7:c.2723A= (DPYD)	ENSP00000359211.3:p.Lys908=
NM_000110.3:c.2723A= , LRG_722t1:c.2723A= (DPYD)	NP_000101.2:p.Lys908=
NR_046590.1:n.64+2546T= (DPYD-AS1)
XM_005270562.3:c.2507A= (DPYD)	XP_005270619.2:p.Lys836=
XM_017000507.1:c.2612A= (DPYD)	XP_016855996.1:p.Lys871=
XM_017000508.2:c.2228A= (DPYD)	XP_016855997.1:p.Lys743=
XM_017000509.2:c.2228A= (DPYD)	XP_016855998.1:p.Lys743=
XM_017000510.1:c.2228A= (DPYD)	XP_016855999.1:p.Lys743=
NM_000110.4:c.2723A= (DPYD) MANE Select	NP_000101.2:p.Lys908=