Canonical Allele Identifier: CA1182917444

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97549697_97549698delinsCT , CM000663.2:g.97549697_97549698delinsCT	GRCh38
NC_000001.10:g.98015253_98015254delinsCT , CM000663.1:g.98015253_98015254delinsCT	GRCh37
NC_000001.9:g.97787841_97787842delinsCT	NCBI36
NG_008807.2:g.376362_376363delinsAG , LRG_722:g.376362_376363delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1386_1387delinsAG MANE Select	ENSP00000359211.3:p.Pro462=
ENST00000370192.7:c.1386_1387delinsAG	ENSP00000359211.3:p.Pro462=
NM_000110.3:c.1386_1387delinsAG , LRG_722t1:c.1386_1387delinsAG	NP_000101.2:p.Pro462=
XM_005270562.3:c.1386_1387delinsAG	XP_005270619.2:p.Pro462=
XM_006710397.2:c.1386_1387delinsAG	XP_006710460.1:p.Pro462=
XM_006710397.3:c.1386_1387delinsAG	XP_006710460.1:p.Pro462=
XM_017000507.1:c.1275_1276delinsAG	XP_016855996.1:p.Pro425=
XM_017000508.2:c.891_892delinsAG	XP_016855997.1:p.Pro297=
XM_017000509.2:c.891_892delinsAG	XP_016855998.1:p.Pro297=
XM_017000510.1:c.891_892delinsAG	XP_016855999.1:p.Pro297=
NM_000110.4:c.1386_1387delinsAG MANE Select	NP_000101.2:p.Pro462=