Canonical Allele Identifier: CA228137

Gene: DPYD

Linked Data

• ClinVar Variation Id: 100099
• ClinVar RCV Id: RCV000086482
• dbSNP Id: rs61789183
• gnomAD v2: 1-98015406-A-T
• gnomAD v3: 1-97549850-A-T
• gnomAD v4: 1-97549850-A-T
• MyVariant Identifiers: chr1:g.98015406A>T (hg19) ; chr1:g.97549850A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97549850A>T , CM000663.2:g.97549850A>T	GRCh38
NC_000001.10:g.98015406A>T , CM000663.1:g.98015406A>T	GRCh37
NC_000001.9:g.97787994A>T	NCBI36
NG_008807.2:g.376210T>A , LRG_722:g.376210T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1340-106T>A MANE Select	ENSP00000359211.3:n.1340-106T>A
ENST00000370192.7:c.1340-106T>A	ENSP00000359211.3:n.1340-106T>A
NM_000110.3:c.1340-106T>A , LRG_722t1:c.1340-106T>A	NP_000101.2:n.1340-106T>A
XM_005270562.3:c.1340-106T>A	XP_005270619.2:n.1340-106T>A
XM_006710397.2:c.1340-106T>A	XP_006710460.1:n.1340-106T>A
XM_006710397.3:c.1340-106T>A	XP_006710460.1:n.1340-106T>A
XM_017000507.1:c.1229-106T>A	XP_016855996.1:n.1229-106T>A
XM_017000508.2:c.845-106T>A	XP_016855997.1:n.845-106T>A
XM_017000509.2:c.845-106T>A	XP_016855998.1:n.845-106T>A
XM_017000510.1:c.845-106T>A	XP_016855999.1:n.845-106T>A
NM_000110.4:c.1340-106T>A MANE Select	NP_000101.2:n.1340-106T>A