Canonical Allele Identifier: CA419147883

Gene: DPYD

Linked Data

• MyVariant Identifiers: chr1:g.98157303C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97691747C>T , CM000663.2:g.97691747C>T	GRCh38
NC_000001.10:g.98157303C>T , CM000663.1:g.98157303C>T	GRCh37
NC_000001.9:g.97929891C>T	NCBI36
NG_008807.2:g.234313G>A , LRG_722:g.234313G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.732G>A MANE Select	ENSP00000359211.3:p.Glu244=
ENST00000370192.7:c.732G>A	ENSP00000359211.3:p.Glu244=
ENST00000474241.1:n.496G>A
NM_000110.3:c.732G>A , LRG_722t1:c.732G>A	NP_000101.2:p.Glu244=
XM_005270562.3:c.732G>A	XP_005270619.2:p.Glu244=
XM_006710397.2:c.732G>A	XP_006710460.1:p.Glu244=
XM_006710397.3:c.732G>A	XP_006710460.1:p.Glu244=
XM_017000507.1:c.621G>A	XP_016855996.1:p.Glu207=
XM_017000508.2:c.237G>A	XP_016855997.1:p.Glu79=
XM_017000509.2:c.237G>A	XP_016855998.1:p.Glu79=
XM_017000510.1:c.237G>A	XP_016855999.1:p.Glu79=
NM_000110.4:c.732G>A MANE Select	NP_000101.2:p.Glu244=