Canonical Allele Identifier: CA1182917364

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97549513_97549520delinsCTTATCCA , CM000663.2:g.97549513_97549520delinsCTTATCCA	GRCh38
NC_000001.10:g.98015069_98015076delinsCTTATCCA , CM000663.1:g.98015069_98015076delinsCTTATCCA	GRCh37
NC_000001.9:g.97787657_97787664delinsCTTATCCA	NCBI36
NG_008807.2:g.376540_376547delinsTGGATAAG , LRG_722:g.376540_376547delinsTGGATAAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.1524+40_1524+47delinsTGGATAAG MANE Select	ENSP00000359211.3:n.1524+40_1524+47delins...
ENST00000370192.7:c.1524+40_1524+47delinsTGGATAAG	ENSP00000359211.3:n.1524+40_1524+47delins...
NM_000110.3:c.1524+40_1524+47delinsTGGATAAG , LRG_722t1:c.1524+40_1524+47delinsTGGATAAG	NP_000101.2:n.1524+40_1524+47delinsTGGATA...
XM_005270562.3:c.1524+40_1524+47delinsTGGATAAG	XP_005270619.2:n.1524+40_1524+47delinsTGG...
XM_006710397.2:c.1524+40_1524+47delinsTGGATAAG	XP_006710460.1:n.1524+40_1524+47delinsTGG...
XM_006710397.3:c.1524+40_1524+47delinsTGGATAAG	XP_006710460.1:n.1524+40_1524+47delinsTGG...
XM_017000507.1:c.1413+40_1413+47delinsTGGATAAG	XP_016855996.1:n.1413+40_1413+47delinsTGG...
XM_017000508.2:c.1029+40_1029+47delinsTGGATAAG	XP_016855997.1:n.1029+40_1029+47delinsTGG...
XM_017000509.2:c.1029+40_1029+47delinsTGGATAAG	XP_016855998.1:n.1029+40_1029+47delinsTGG...
XM_017000510.1:c.1029+40_1029+47delinsTGGATAAG	XP_016855999.1:n.1029+40_1029+47delinsTGG...
NM_000110.4:c.1524+40_1524+47delinsTGGATAAG MANE Select	NP_000101.2:n.1524+40_1524+47delinsTGGATA...