Canonical Allele Identifier: CA2744701773

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97549799_97549800insCACACCCAAC , CM000663.2:g.97549799_97549800insCACACCCAAC	GRCh38
NC_000001.10:g.98015355_98015356insCACACCCAAC , CM000663.1:g.98015355_98015356insCACACCCAAC	GRCh37
NC_000001.9:g.97787943_97787944insCACACCCAAC	NCBI36
NG_008807.2:g.376260_376261insGTTGGGTGTG , LRG_722:g.376260_376261insGTTGGGTGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1340-56_1340-55insGTTGGGTGTG MANE Select	ENSP00000359211.3:n.1340-56_1340-55insGTTGGGTGTG
ENST00000370192.7:c.1340-56_1340-55insGTTGGGTGTG	ENSP00000359211.3:n.1340-56_1340-55insGTTGGGTGTG
NM_000110.3:c.1340-56_1340-55insGTTGGGTGTG , LRG_722t1:c.1340-56_1340-55insGTTGGGTGTG	NP_000101.2:n.1340-56_1340-55insGTTGGGTGTG
XM_005270562.3:c.1340-56_1340-55insGTTGGGTGTG	XP_005270619.2:n.1340-56_1340-55insGTTGGGTGTG
XM_006710397.2:c.1340-56_1340-55insGTTGGGTGTG	XP_006710460.1:n.1340-56_1340-55insGTTGGGTGTG
XM_006710397.3:c.1340-56_1340-55insGTTGGGTGTG	XP_006710460.1:n.1340-56_1340-55insGTTGGGTGTG
XM_017000507.1:c.1229-56_1229-55insGTTGGGTGTG	XP_016855996.1:n.1229-56_1229-55insGTTGGGTGTG
XM_017000508.2:c.845-56_845-55insGTTGGGTGTG	XP_016855997.1:n.845-56_845-55insGTTGGGTGTG
XM_017000509.2:c.845-56_845-55insGTTGGGTGTG	XP_016855998.1:n.845-56_845-55insGTTGGGTGTG
XM_017000510.1:c.845-56_845-55insGTTGGGTGTG	XP_016855999.1:n.845-56_845-55insGTTGGGTGTG
NM_000110.4:c.1340-56_1340-55insGTTGGGTGTG MANE Select	NP_000101.2:n.1340-56_1340-55insGTTGGGTGTG