Canonical Allele Identifier: CA1182917441

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97549695_97549709delinsTTCTGGGAGACCCCA , CM000663.2:g.97549695_97549709delinsTTCTGGGAGACCCCA	GRCh38
NC_000001.10:g.98015251_98015265delinsTTCTGGGAGACCCCA , CM000663.1:g.98015251_98015265delinsTTCTGGGAGACCCCA	GRCh37
NC_000001.9:g.97787839_97787853delinsTTCTGGGAGACCCCA	NCBI36
NG_008807.2:g.376351_376365delinsTGGGGTCTCCCAGAA , LRG_722:g.376351_376365delinsTGGGGTCTCCCAGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1375_1389delinsTGGGGTCTCCCAGAA MANE Select	ENSP00000359211.3:p.Trp459=
ENST00000370192.7:c.1375_1389delinsTGGGGTCTCCCAGAA	ENSP00000359211.3:p.Trp459=
NM_000110.3:c.1375_1389delinsTGGGGTCTCCCAGAA , LRG_722t1:c.1375_1389delinsTGGGGTCTCCCAGAA	NP_000101.2:p.Trp459=
XM_005270562.3:c.1375_1389delinsTGGGGTCTCCCAGAA	XP_005270619.2:p.Trp459=
XM_006710397.2:c.1375_1389delinsTGGGGTCTCCCAGAA	XP_006710460.1:p.Trp459=
XM_006710397.3:c.1375_1389delinsTGGGGTCTCCCAGAA	XP_006710460.1:p.Trp459=
XM_017000507.1:c.1264_1278delinsTGGGGTCTCCCAGAA	XP_016855996.1:p.Trp422=
XM_017000508.2:c.880_894delinsTGGGGTCTCCCAGAA	XP_016855997.1:p.Trp294=
XM_017000509.2:c.880_894delinsTGGGGTCTCCCAGAA	XP_016855998.1:p.Trp294=
XM_017000510.1:c.880_894delinsTGGGGTCTCCCAGAA	XP_016855999.1:p.Trp294=
NM_000110.4:c.1375_1389delinsTGGGGTCTCCCAGAA MANE Select	NP_000101.2:p.Trp459=