Canonical Allele Identifier: CA524781020

Gene: DPYD DPYD-AS1

Linked Data

• dbSNP Id: rs1282340496
• gnomAD v2: 1-97770917-T-TAA
• gnomAD v3: 1-97305361-T-TAA
• gnomAD v4: 1-97305361-T-TAA
• MyVariant Identifiers: chr1:g.97770917_97770918insAA (hg19) ; chr1:g.97305361_97305362insAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97305362_97305363dup , CM000663.2:g.97305362_97305363dup	GRCh38
NC_000001.10:g.97770918_97770919dup , CM000663.1:g.97770918_97770919dup	GRCh37
NC_000001.9:g.97543506_97543507dup	NCBI36
NG_008807.2:g.620697_620698dup , LRG_722:g.620697_620698dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2195_2196dup (DPYD) MANE Select	ENSP00000359211.3:p.Thr733LeufsTer10
ENST00000370192.7:c.2195_2196dup (DPYD)	ENSP00000359211.3:p.Thr733LeufsTer10
NM_000110.3:c.2195_2196dup , LRG_722t1:c.2195_2196dup (DPYD)	NP_000101.2:p.Thr733LeufsTer10
NR_046590.1:n.129-827_129-826dup (DPYD-AS1)
XM_005270562.3:c.1979_1980dup (DPYD)	XP_005270619.2:p.Thr661LeufsTer10
XM_006710397.2:c.2195_2196dup (DPYD)	XP_006710460.1:p.Thr733LeufsTer10
XM_006710397.3:c.2195_2196dup (DPYD)	XP_006710460.1:p.Thr733LeufsTer10
XM_017000507.1:c.2084_2085dup (DPYD)	XP_016855996.1:p.Thr696LeufsTer10
XM_017000508.2:c.1700_1701dup (DPYD)	XP_016855997.1:p.Thr568LeufsTer10
XM_017000509.2:c.1700_1701dup (DPYD)	XP_016855998.1:p.Thr568LeufsTer10
XM_017000510.1:c.1700_1701dup (DPYD)	XP_016855999.1:p.Thr568LeufsTer10
NM_000110.4:c.2195_2196dup (DPYD) MANE Select	NP_000101.2:p.Thr733LeufsTer10