Canonical Allele Identifier: CA2519489333

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97691180_97691183del , CM000663.2:g.97691180_97691183del	GRCh38
NC_000001.10:g.98156736_98156739del , CM000663.1:g.98156736_98156739del	GRCh37
NC_000001.9:g.97929324_97929327del	NCBI36
NG_008807.2:g.234879_234882del , LRG_722:g.234879_234882del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.762+536_762+539del MANE Select	ENSP00000359211.3:n.762+536_762+539del
ENST00000370192.7:c.762+536_762+539del	ENSP00000359211.3:n.762+536_762+539del
NM_000110.3:c.762+536_762+539del , LRG_722t1:c.762+536_762+539del	NP_000101.2:n.762+536_762+539del
XM_005270562.3:c.762+536_762+539del	XP_005270619.2:n.762+536_762+539del
XM_006710397.2:c.762+536_762+539del	XP_006710460.1:n.762+536_762+539del
XM_006710397.3:c.762+536_762+539del	XP_006710460.1:n.762+536_762+539del
XM_017000507.1:c.651+536_651+539del	XP_016855996.1:n.651+536_651+539del
XM_017000508.2:c.267+536_267+539del	XP_016855997.1:n.267+536_267+539del
XM_017000509.2:c.267+536_267+539del	XP_016855998.1:n.267+536_267+539del
XM_017000510.1:c.267+536_267+539del	XP_016855999.1:n.267+536_267+539del
NM_000110.4:c.762+536_762+539del MANE Select	NP_000101.2:n.762+536_762+539del