Canonical Allele Identifier: CA2551308262

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97691406_97691407insTATTTCACA , CM000663.2:g.97691406_97691407insTATTTCACA	GRCh38
NC_000001.10:g.98156962_98156963insTATTTCACA , CM000663.1:g.98156962_98156963insTATTTCACA	GRCh37
NC_000001.9:g.97929550_97929551insTATTTCACA	NCBI36
NG_008807.2:g.234653_234654insTGTGAAATA , LRG_722:g.234653_234654insTGTGAAATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.762+310_762+311insTGTGAAATA MANE Select	ENSP00000359211.3:n.762+310_762+311insTGTGAAATA
ENST00000370192.7:c.762+310_762+311insTGTGAAATA	ENSP00000359211.3:n.762+310_762+311insTGTGAAATA
ENST00000474241.1:n.836_837insTGTGAAATA
NM_000110.3:c.762+310_762+311insTGTGAAATA , LRG_722t1:c.762+310_762+311insTGTGAAATA	NP_000101.2:n.762+310_762+311insTGTGAAATA
XM_005270562.3:c.762+310_762+311insTGTGAAATA	XP_005270619.2:n.762+310_762+311insTGTGAAATA
XM_006710397.2:c.762+310_762+311insTGTGAAATA	XP_006710460.1:n.762+310_762+311insTGTGAAATA
XM_006710397.3:c.762+310_762+311insTGTGAAATA	XP_006710460.1:n.762+310_762+311insTGTGAAATA
XM_017000507.1:c.651+310_651+311insTGTGAAATA	XP_016855996.1:n.651+310_651+311insTGTGAAATA
XM_017000508.2:c.267+310_267+311insTGTGAAATA	XP_016855997.1:n.267+310_267+311insTGTGAAATA
XM_017000509.2:c.267+310_267+311insTGTGAAATA	XP_016855998.1:n.267+310_267+311insTGTGAAATA
XM_017000510.1:c.267+310_267+311insTGTGAAATA	XP_016855999.1:n.267+310_267+311insTGTGAAATA
NM_000110.4:c.762+310_762+311insTGTGAAATA MANE Select	NP_000101.2:n.762+310_762+311insTGTGAAATA