Canonical Allele Identifier: CA1182917567

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97549938_97549939delinsCT , CM000663.2:g.97549938_97549939delinsCT	GRCh38
NC_000001.10:g.98015494_98015495delinsCT , CM000663.1:g.98015494_98015495delinsCT	GRCh37
NC_000001.9:g.97788082_97788083delinsCT	NCBI36
NG_008807.2:g.376121_376122delinsAG , LRG_722:g.376121_376122delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1340-195_1340-194delinsAG MANE Select	ENSP00000359211.3:n.1340-195_1340-194delinsAG
ENST00000370192.7:c.1340-195_1340-194delinsAG	ENSP00000359211.3:n.1340-195_1340-194delinsAG
NM_000110.3:c.1340-195_1340-194delinsAG , LRG_722t1:c.1340-195_1340-194delinsAG	NP_000101.2:n.1340-195_1340-194delinsAG
XM_005270562.3:c.1340-195_1340-194delinsAG	XP_005270619.2:n.1340-195_1340-194delinsAG
XM_006710397.2:c.1340-195_1340-194delinsAG	XP_006710460.1:n.1340-195_1340-194delinsAG
XM_006710397.3:c.1340-195_1340-194delinsAG	XP_006710460.1:n.1340-195_1340-194delinsAG
XM_017000507.1:c.1229-195_1229-194delinsAG	XP_016855996.1:n.1229-195_1229-194delinsAG
XM_017000508.2:c.845-195_845-194delinsAG	XP_016855997.1:n.845-195_845-194delinsAG
XM_017000509.2:c.845-195_845-194delinsAG	XP_016855998.1:n.845-195_845-194delinsAG
XM_017000510.1:c.845-195_845-194delinsAG	XP_016855999.1:n.845-195_845-194delinsAG
NM_000110.4:c.1340-195_1340-194delinsAG MANE Select	NP_000101.2:n.1340-195_1340-194delinsAG