Canonical Allele Identifier: CA341379180

Gene: DPYD

Linked Data

• dbSNP Id: rs1661017978
• gnomAD v3: 1-97691718-T-C
• gnomAD v4: 1-97691718-T-C
• MyVariant Identifiers: chr1:g.98157274T>C (hg19) ; chr1:g.97691718T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97691718T>C , CM000663.2:g.97691718T>C	GRCh38
NC_000001.10:g.98157274T>C , CM000663.1:g.98157274T>C	GRCh37
NC_000001.9:g.97929862T>C	NCBI36
NG_008807.2:g.234342A>G , LRG_722:g.234342A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.761A>G MANE Select	ENSP00000359211.3:p.Lys254Arg
ENST00000370192.7:c.761A>G	ENSP00000359211.3:p.Lys254Arg
ENST00000474241.1:n.525A>G
NM_000110.3:c.761A>G , LRG_722t1:c.761A>G	NP_000101.2:p.Lys254Arg
XM_005270562.3:c.761A>G	XP_005270619.2:p.Lys254Arg
XM_006710397.2:c.761A>G	XP_006710460.1:p.Lys254Arg
XM_006710397.3:c.761A>G	XP_006710460.1:p.Lys254Arg
XM_017000507.1:c.650A>G	XP_016855996.1:p.Lys217Arg
XM_017000508.2:c.266A>G	XP_016855997.1:p.Lys89Arg
XM_017000509.2:c.266A>G	XP_016855998.1:p.Lys89Arg
XM_017000510.1:c.266A>G	XP_016855999.1:p.Lys89Arg
NM_000110.4:c.761A>G MANE Select	NP_000101.2:p.Lys254Arg