Canonical Allele Identifier: CA341378275

Gene: DPYD

Linked Data

• dbSNP Id: rs2101975587
• MyVariant Identifiers: chr1:g.97981337C>T (hg19) ; chr1:g.97515781C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97515781C>T , CM000663.2:g.97515781C>T	GRCh38
NC_000001.10:g.97981337C>T , CM000663.1:g.97981337C>T	GRCh37
NC_000001.9:g.97753925C>T	NCBI36
NG_008807.2:g.410279G>A , LRG_722:g.410279G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1685G>A MANE Select	ENSP00000359211.3:p.Arg562Lys
ENST00000370192.7:c.1685G>A	ENSP00000359211.3:p.Arg562Lys
NM_000110.3:c.1685G>A , LRG_722t1:c.1685G>A	NP_000101.2:p.Arg562Lys
XM_005270562.3:c.1524+33779G>A	XP_005270619.2:n.1524+33779G>A
XM_006710397.2:c.1685G>A	XP_006710460.1:p.Arg562Lys
XM_006710397.3:c.1685G>A	XP_006710460.1:p.Arg562Lys
XM_017000507.1:c.1574G>A	XP_016855996.1:p.Arg525Lys
XM_017000508.2:c.1190G>A	XP_016855997.1:p.Arg397Lys
XM_017000509.2:c.1190G>A	XP_016855998.1:p.Arg397Lys
XM_017000510.1:c.1190G>A	XP_016855999.1:p.Arg397Lys
NM_000110.4:c.1685G>A MANE Select	NP_000101.2:p.Arg562Lys