Canonical Allele Identifier: CA419148271

Gene: DPYD

Linked Data

• MyVariant Identifiers: chr1:g.98293693T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97828137T>A , CM000663.2:g.97828137T>A	GRCh38
NC_000001.10:g.98293693T>A , CM000663.1:g.98293693T>A	GRCh37
NC_000001.9:g.98066281T>A	NCBI36
NG_008807.2:g.97923A>T , LRG_722:g.97923A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.210A>T MANE Select	ENSP00000359211.3:p.Arg70=
ENST00000306031.5:c.210A>T	ENSP00000307107.5:p.Arg70=
ENST00000370192.7:c.210A>T	ENSP00000359211.3:p.Arg70=
NM_000110.3:c.210A>T , LRG_722t1:c.210A>T	NP_000101.2:p.Arg70=
NM_001160301.1:c.210A>T , LRG_722t2:c.210A>T	NP_001153773.1:p.Arg70=
XM_005270562.3:c.210A>T	XP_005270619.2:p.Arg70=
XM_006710397.2:c.210A>T	XP_006710460.1:p.Arg70=
XM_006710397.3:c.210A>T	XP_006710460.1:p.Arg70=
XM_017000507.1:c.99A>T	XP_016855996.1:p.Arg33=
XM_017000508.2:c.-501A>T	XP_016855997.1:n.-501A>T
XM_017000509.2:c.-399A>T	XP_016855998.1:n.-399A>T
XM_017000510.1:c.-399A>T	XP_016855999.1:n.-399A>T
XR_001737014.1:n.347A>T
NM_000110.4:c.210A>T MANE Select	NP_000101.2:p.Arg70=