Canonical Allele Identifier: CA1182717217

Gene: DPYD DPYD-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97098608G= , CM000663.2:g.97098608G=	GRCh38
NC_000001.10:g.97564164G= , CM000663.1:g.97564164G=	GRCh37
NC_000001.9:g.97336752G=	NCBI36
NG_008807.2:g.827452C= , LRG_722:g.827452C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2647C= (DPYD) MANE Select	ENSP00000359211.3:p.Leu883=
ENST00000370192.7:c.2647C= (DPYD)	ENSP00000359211.3:p.Leu883=
NM_000110.3:c.2647C= , LRG_722t1:c.2647C= (DPYD)	NP_000101.2:p.Leu883=
NR_046590.1:n.64+2622G= (DPYD-AS1)
XM_005270562.3:c.2431C= (DPYD)	XP_005270619.2:p.Leu811=
XM_017000507.1:c.2536C= (DPYD)	XP_016855996.1:p.Leu846=
XM_017000508.2:c.2152C= (DPYD)	XP_016855997.1:p.Leu718=
XM_017000509.2:c.2152C= (DPYD)	XP_016855998.1:p.Leu718=
XM_017000510.1:c.2152C= (DPYD)	XP_016855999.1:p.Leu718=
NM_000110.4:c.2647C= (DPYD) MANE Select	NP_000101.2:p.Leu883=