Canonical Allele Identifier: CA2574442273

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97549693_97549695del , CM000663.2:g.97549693_97549695del	GRCh38
NC_000001.10:g.98015249_98015251del , CM000663.1:g.98015249_98015251del	GRCh37
NC_000001.9:g.97787837_97787839del	NCBI36
NG_008807.2:g.376367_376369del , LRG_722:g.376367_376369del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1391_1393del MANE Select	ENSP00000359211.3:p.Val464del
ENST00000370192.7:c.1391_1393del	ENSP00000359211.3:p.Val464del
NM_000110.3:c.1391_1393del , LRG_722t1:c.1391_1393del	NP_000101.2:p.Val464del
XM_005270562.3:c.1391_1393del	XP_005270619.2:p.Val464del
XM_006710397.2:c.1391_1393del	XP_006710460.1:p.Val464del
XM_006710397.3:c.1391_1393del	XP_006710460.1:p.Val464del
XM_017000507.1:c.1280_1282del	XP_016855996.1:p.Val427del
XM_017000508.2:c.896_898del	XP_016855997.1:p.Val299del
XM_017000509.2:c.896_898del	XP_016855998.1:p.Val299del
XM_017000510.1:c.896_898del	XP_016855999.1:p.Val299del
NM_000110.4:c.1391_1393del MANE Select	NP_000101.2:p.Val464del