Canonical Allele Identifier: CA1182717191

Gene: DPYD DPYD-AS1

Linked Data

• ClinVar Variation Id: 2674914
• ClinVar RCV Id: RCV003459989
• dbSNP Id: rs1650431372
• gnomAD v4: 1-97098521-AAC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97098523_97098524del , CM000663.2:g.97098523_97098524del	GRCh38
NC_000001.10:g.97564079_97564080del , CM000663.1:g.97564079_97564080del	GRCh37
NC_000001.9:g.97336667_97336668del	NCBI36
NG_008807.2:g.827537_827538del , LRG_722:g.827537_827538del

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.2732_2733del (DPYD) MANE Select	ENSP00000359211.3:p.Cys911PhefsTer26
ENST00000370192.7:c.2732_2733del (DPYD)	ENSP00000359211.3:p.Cys911PhefsTer26
NM_000110.3:c.2732_2733del , LRG_722t1:c.2732_2733del (DPYD)	NP_000101.2:p.Cys911PhefsTer26
NR_046590.1:n.64+2537_64+2538del (DPYD-AS1)
XM_005270562.3:c.2516_2517del (DPYD)	XP_005270619.2:p.Cys839PhefsTer26
XM_017000507.1:c.2621_2622del (DPYD)	XP_016855996.1:p.Cys874PhefsTer26
XM_017000508.2:c.2237_2238del (DPYD)	XP_016855997.1:p.Cys746PhefsTer26
XM_017000509.2:c.2237_2238del (DPYD)	XP_016855998.1:p.Cys746PhefsTer26
XM_017000510.1:c.2237_2238del (DPYD)	XP_016855999.1:p.Cys746PhefsTer26
NM_000110.4:c.2732_2733del (DPYD) MANE Select	NP_000101.2:p.Cys911PhefsTer26