Canonical Allele Identifier: CA341377677

Gene: DPYD

Linked Data

• gnomAD v4: 1-97549642-T-A
• MyVariant Identifiers: chr1:g.98015198T>A (hg19) ; chr1:g.97549642T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97549642T>A , CM000663.2:g.97549642T>A	GRCh38
NC_000001.10:g.98015198T>A , CM000663.1:g.98015198T>A	GRCh37
NC_000001.9:g.97787786T>A	NCBI36
NG_008807.2:g.376418A>T , LRG_722:g.376418A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1442A>T MANE Select	ENSP00000359211.3:p.Asp481Val
ENST00000370192.7:c.1442A>T	ENSP00000359211.3:p.Asp481Val
NM_000110.3:c.1442A>T , LRG_722t1:c.1442A>T	NP_000101.2:p.Asp481Val
XM_005270562.3:c.1442A>T	XP_005270619.2:p.Asp481Val
XM_006710397.2:c.1442A>T	XP_006710460.1:p.Asp481Val
XM_006710397.3:c.1442A>T	XP_006710460.1:p.Asp481Val
XM_017000507.1:c.1331A>T	XP_016855996.1:p.Asp444Val
XM_017000508.2:c.947A>T	XP_016855997.1:p.Asp316Val
XM_017000509.2:c.947A>T	XP_016855998.1:p.Asp316Val
XM_017000510.1:c.947A>T	XP_016855999.1:p.Asp316Val
NM_000110.4:c.1442A>T MANE Select	NP_000101.2:p.Asp481Val