Canonical Allele Identifier: CA341376018

Gene: DPYD

Linked Data

• MyVariant Identifiers: chr1:g.97915667G>T (hg19) ; chr1:g.97450111G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97450111G>T , CM000663.2:g.97450111G>T	GRCh38
NC_000001.10:g.97915667G>T , CM000663.1:g.97915667G>T	GRCh37
NC_000001.9:g.97688255G>T	NCBI36
NG_008807.2:g.475949C>A , LRG_722:g.475949C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.1853C>A MANE Select	ENSP00000359211.3:p.Ala618Asp
ENST00000370192.7:c.1853C>A	ENSP00000359211.3:p.Ala618Asp
NM_000110.3:c.1853C>A , LRG_722t1:c.1853C>A	NP_000101.2:p.Ala618Asp
XM_005270562.3:c.1637C>A	XP_005270619.2:p.Ala546Asp
XM_006710397.2:c.1853C>A	XP_006710460.1:p.Ala618Asp
XM_006710397.3:c.1853C>A	XP_006710460.1:p.Ala618Asp
XM_017000507.1:c.1742C>A	XP_016855996.1:p.Ala581Asp
XM_017000508.2:c.1358C>A	XP_016855997.1:p.Ala453Asp
XM_017000509.2:c.1358C>A	XP_016855998.1:p.Ala453Asp
XM_017000510.1:c.1358C>A	XP_016855999.1:p.Ala453Asp
NM_000110.4:c.1853C>A MANE Select	NP_000101.2:p.Ala618Asp