Canonical Allele Identifier: CA2744701768

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97549572del , CM000663.2:g.97549572del	GRCh38
NC_000001.10:g.98015128del , CM000663.1:g.98015128del	GRCh37
NC_000001.9:g.97787716del	NCBI36
NG_008807.2:g.376488del , LRG_722:g.376488del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1512del MANE Select	ENSP00000359211.3:p.His504GlnfsTer?
ENST00000370192.7:c.1512del	ENSP00000359211.3:p.His504GlnfsTer?
NM_000110.3:c.1512del , LRG_722t1:c.1512del	NP_000101.2:p.His504GlnfsTer?
XM_005270562.3:c.1512del	XP_005270619.2:p.His504GlnfsTer8
XM_006710397.2:c.1512del	XP_006710460.1:p.His504GlnfsTer?
XM_006710397.3:c.1512del	XP_006710460.1:p.His504GlnfsTer?
XM_017000507.1:c.1401del	XP_016855996.1:p.His467GlnfsTer?
XM_017000508.2:c.1017del	XP_016855997.1:p.His339GlnfsTer?
XM_017000509.2:c.1017del	XP_016855998.1:p.His339GlnfsTer?
XM_017000510.1:c.1017del	XP_016855999.1:p.His339GlnfsTer?
NM_000110.4:c.1512del MANE Select	NP_000101.2:p.His504GlnfsTer?