Canonical Allele Identifier: CA341375944

Gene: DPYD

Linked Data

• dbSNP Id: rs2101792083
• gnomAD v4: 1-97450078-T-A
• MyVariant Identifiers: chr1:g.97915634T>A (hg19) ; chr1:g.97450078T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97450078T>A , CM000663.2:g.97450078T>A	GRCh38
NC_000001.10:g.97915634T>A , CM000663.1:g.97915634T>A	GRCh37
NC_000001.9:g.97688222T>A	NCBI36
NG_008807.2:g.475982A>T , LRG_722:g.475982A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1886A>T MANE Select	ENSP00000359211.3:p.Lys629Met
ENST00000370192.7:c.1886A>T	ENSP00000359211.3:p.Lys629Met
NM_000110.3:c.1886A>T , LRG_722t1:c.1886A>T	NP_000101.2:p.Lys629Met
XM_005270562.3:c.1670A>T	XP_005270619.2:p.Lys557Met
XM_006710397.2:c.1886A>T	XP_006710460.1:p.Lys629Met
XM_006710397.3:c.1886A>T	XP_006710460.1:p.Lys629Met
XM_017000507.1:c.1775A>T	XP_016855996.1:p.Lys592Met
XM_017000508.2:c.1391A>T	XP_016855997.1:p.Lys464Met
XM_017000509.2:c.1391A>T	XP_016855998.1:p.Lys464Met
XM_017000510.1:c.1391A>T	XP_016855999.1:p.Lys464Met
NM_000110.4:c.1886A>T MANE Select	NP_000101.2:p.Lys629Met