Canonical Allele Identifier: CA341379193

Gene: DPYD

Linked Data

• dbSNP Id: rs1214282631
• gnomAD v3: 1-97691724-C-T
• gnomAD v4: 1-97691724-C-T
• MyVariant Identifiers: chr1:g.98157280C>T (hg19) ; chr1:g.97691724C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97691724C>T , CM000663.2:g.97691724C>T	GRCh38
NC_000001.10:g.98157280C>T , CM000663.1:g.98157280C>T	GRCh37
NC_000001.9:g.97929868C>T	NCBI36
NG_008807.2:g.234336G>A , LRG_722:g.234336G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.755G>A MANE Select	ENSP00000359211.3:p.Gly252Asp
ENST00000370192.7:c.755G>A	ENSP00000359211.3:p.Gly252Asp
ENST00000474241.1:n.519G>A
NM_000110.3:c.755G>A , LRG_722t1:c.755G>A	NP_000101.2:p.Gly252Asp
XM_005270562.3:c.755G>A	XP_005270619.2:p.Gly252Asp
XM_006710397.2:c.755G>A	XP_006710460.1:p.Gly252Asp
XM_006710397.3:c.755G>A	XP_006710460.1:p.Gly252Asp
XM_017000507.1:c.644G>A	XP_016855996.1:p.Gly215Asp
XM_017000508.2:c.260G>A	XP_016855997.1:p.Gly87Asp
XM_017000509.2:c.260G>A	XP_016855998.1:p.Gly87Asp
XM_017000510.1:c.260G>A	XP_016855999.1:p.Gly87Asp
NM_000110.4:c.755G>A MANE Select	NP_000101.2:p.Gly252Asp