Canonical Allele Identifier: CA1182917469

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97549764_97549775delinsACAATAGACAAT , CM000663.2:g.97549764_97549775delinsACAATAGACAAT	GRCh38
NC_000001.10:g.98015320_98015331delinsACAATAGACAAT , CM000663.1:g.98015320_98015331delinsACAATAGACAAT	GRCh37
NC_000001.9:g.97787908_97787919delinsACAATAGACAAT	NCBI36
NG_008807.2:g.376285_376296delinsATTGTCTATTGT , LRG_722:g.376285_376296delinsATTGTCTATTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1340-31_1340-20delinsATTGTCTATTGT MANE Select	ENSP00000359211.3:n.1340-31_1340-20delinsATTGTCTATTGT
ENST00000370192.7:c.1340-31_1340-20delinsATTGTCTATTGT	ENSP00000359211.3:n.1340-31_1340-20delinsATTGTCTATTGT
NM_000110.3:c.1340-31_1340-20delinsATTGTCTATTGT , LRG_722t1:c.1340-31_1340-20delinsATTGTCTATTGT	NP_000101.2:n.1340-31_1340-20delinsATTGTCTATTGT
XM_005270562.3:c.1340-31_1340-20delinsATTGTCTATTGT	XP_005270619.2:n.1340-31_1340-20delinsATTGTCTATTGT
XM_006710397.2:c.1340-31_1340-20delinsATTGTCTATTGT	XP_006710460.1:n.1340-31_1340-20delinsATTGTCTATTGT
XM_006710397.3:c.1340-31_1340-20delinsATTGTCTATTGT	XP_006710460.1:n.1340-31_1340-20delinsATTGTCTATTGT
XM_017000507.1:c.1229-31_1229-20delinsATTGTCTATTGT	XP_016855996.1:n.1229-31_1229-20delinsATTGTCTATTGT
XM_017000508.2:c.845-31_845-20delinsATTGTCTATTGT	XP_016855997.1:n.845-31_845-20delinsATTGTCTATTGT
XM_017000509.2:c.845-31_845-20delinsATTGTCTATTGT	XP_016855998.1:n.845-31_845-20delinsATTGTCTATTGT
XM_017000510.1:c.845-31_845-20delinsATTGTCTATTGT	XP_016855999.1:n.845-31_845-20delinsATTGTCTATTGT
NM_000110.4:c.1340-31_1340-20delinsATTGTCTATTGT MANE Select	NP_000101.2:n.1340-31_1340-20delinsATTGTCTATTGT