Canonical Allele Identifier: CA1182917388

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97549565_97549566delinsCG , CM000663.2:g.97549565_97549566delinsCG	GRCh38
NC_000001.10:g.98015121_98015122delinsCG , CM000663.1:g.98015121_98015122delinsCG	GRCh37
NC_000001.9:g.97787709_97787710delinsCG	NCBI36
NG_008807.2:g.376494_376495delinsCG , LRG_722:g.376494_376495delinsCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.1518_1519delinsCG MANE Select	ENSP00000359211.3:p.Tyr506=
ENST00000370192.7:c.1518_1519delinsCG	ENSP00000359211.3:p.Tyr506=
NM_000110.3:c.1518_1519delinsCG , LRG_722t1:c.1518_1519delinsCG	NP_000101.2:p.Tyr506=
XM_005270562.3:c.1518_1519delinsCG	XP_005270619.2:p.Tyr506=
XM_006710397.2:c.1518_1519delinsCG	XP_006710460.1:p.Tyr506=
XM_006710397.3:c.1518_1519delinsCG	XP_006710460.1:p.Tyr506=
XM_017000507.1:c.1407_1408delinsCG	XP_016855996.1:p.Tyr469=
XM_017000508.2:c.1023_1024delinsCG	XP_016855997.1:p.Tyr341=
XM_017000509.2:c.1023_1024delinsCG	XP_016855998.1:p.Tyr341=
XM_017000510.1:c.1023_1024delinsCG	XP_016855999.1:p.Tyr341=
NM_000110.4:c.1518_1519delinsCG MANE Select	NP_000101.2:p.Tyr506=