Canonical Allele Identifier: CA341379195

Gene: DPYD

Linked Data

• dbSNP Id: rs765034707
• MyVariant Identifiers: chr1:g.98157281C>T (hg19) ; chr1:g.97691725C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97691725C>T , CM000663.2:g.97691725C>T	GRCh38
NC_000001.10:g.98157281C>T , CM000663.1:g.98157281C>T	GRCh37
NC_000001.9:g.97929869C>T	NCBI36
NG_008807.2:g.234335G>A , LRG_722:g.234335G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.754G>A MANE Select	ENSP00000359211.3:p.Gly252Ser
ENST00000370192.7:c.754G>A	ENSP00000359211.3:p.Gly252Ser
ENST00000474241.1:n.518G>A
NM_000110.3:c.754G>A , LRG_722t1:c.754G>A	NP_000101.2:p.Gly252Ser
XM_005270562.3:c.754G>A	XP_005270619.2:p.Gly252Ser
XM_006710397.2:c.754G>A	XP_006710460.1:p.Gly252Ser
XM_006710397.3:c.754G>A	XP_006710460.1:p.Gly252Ser
XM_017000507.1:c.643G>A	XP_016855996.1:p.Gly215Ser
XM_017000508.2:c.259G>A	XP_016855997.1:p.Gly87Ser
XM_017000509.2:c.259G>A	XP_016855998.1:p.Gly87Ser
XM_017000510.1:c.259G>A	XP_016855999.1:p.Gly87Ser
NM_000110.4:c.754G>A MANE Select	NP_000101.2:p.Gly252Ser