Canonical Allele Identifier: CA2744701769

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97549592_97549593insTA , CM000663.2:g.97549592_97549593insTA	GRCh38
NC_000001.10:g.98015148_98015149insTA , CM000663.1:g.98015148_98015149insTA	GRCh37
NC_000001.9:g.97787736_97787737insTA	NCBI36
NG_008807.2:g.376467_376468insTA , LRG_722:g.376467_376468insTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1491_1492insTA MANE Select	ENSP00000359211.3:p.Gln498TyrfsTer?
ENST00000370192.7:c.1491_1492insTA	ENSP00000359211.3:p.Gln498TyrfsTer?
NM_000110.3:c.1491_1492insTA , LRG_722t1:c.1491_1492insTA	NP_000101.2:p.Gln498TyrfsTer?
XM_005270562.3:c.1491_1492insTA	XP_005270619.2:p.Gln498TyrfsTer15
XM_006710397.2:c.1491_1492insTA	XP_006710460.1:p.Gln498TyrfsTer?
XM_006710397.3:c.1491_1492insTA	XP_006710460.1:p.Gln498TyrfsTer?
XM_017000507.1:c.1380_1381insTA	XP_016855996.1:p.Gln461TyrfsTer?
XM_017000508.2:c.996_997insTA	XP_016855997.1:p.Gln333TyrfsTer?
XM_017000509.2:c.996_997insTA	XP_016855998.1:p.Gln333TyrfsTer?
XM_017000510.1:c.996_997insTA	XP_016855999.1:p.Gln333TyrfsTer?
NM_000110.4:c.1491_1492insTA MANE Select	NP_000101.2:p.Gln498TyrfsTer?