Canonical Allele Identifier: CA1182917282

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97549292_97549293delinsCG , CM000663.2:g.97549292_97549293delinsCG	GRCh38
NC_000001.10:g.98014848_98014849delinsCG , CM000663.1:g.98014848_98014849delinsCG	GRCh37
NC_000001.9:g.97787436_97787437delinsCG	NCBI36
NG_008807.2:g.376767_376768delinsCG , LRG_722:g.376767_376768delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1524+267_1524+268delinsCG MANE Select	ENSP00000359211.3:n.1524+267_1524+268delinsCG
ENST00000370192.7:c.1524+267_1524+268delinsCG	ENSP00000359211.3:n.1524+267_1524+268delinsCG
NM_000110.3:c.1524+267_1524+268delinsCG , LRG_722t1:c.1524+267_1524+268delinsCG	NP_000101.2:n.1524+267_1524+268delinsCG
XM_005270562.3:c.1524+267_1524+268delinsCG	XP_005270619.2:n.1524+267_1524+268delinsCG
XM_006710397.2:c.1524+267_1524+268delinsCG	XP_006710460.1:n.1524+267_1524+268delinsCG
XM_006710397.3:c.1524+267_1524+268delinsCG	XP_006710460.1:n.1524+267_1524+268delinsCG
XM_017000507.1:c.1413+267_1413+268delinsCG	XP_016855996.1:n.1413+267_1413+268delinsCG
XM_017000508.2:c.1029+267_1029+268delinsCG	XP_016855997.1:n.1029+267_1029+268delinsCG
XM_017000509.2:c.1029+267_1029+268delinsCG	XP_016855998.1:n.1029+267_1029+268delinsCG
XM_017000510.1:c.1029+267_1029+268delinsCG	XP_016855999.1:n.1029+267_1029+268delinsCG
NM_000110.4:c.1524+267_1524+268delinsCG MANE Select	NP_000101.2:n.1524+267_1524+268delinsCG