Canonical Allele Identifier: CA341379299

Gene: DPYD

Linked Data

• MyVariant Identifiers: chr1:g.98157326G>T (hg19) ; chr1:g.97691770G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97691770G>T , CM000663.2:g.97691770G>T	GRCh38
NC_000001.10:g.98157326G>T , CM000663.1:g.98157326G>T	GRCh37
NC_000001.9:g.97929914G>T	NCBI36
NG_008807.2:g.234290C>A , LRG_722:g.234290C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.709C>A MANE Select	ENSP00000359211.3:p.Pro237Thr
ENST00000370192.7:c.709C>A	ENSP00000359211.3:p.Pro237Thr
ENST00000474241.1:n.473C>A
NM_000110.3:c.709C>A , LRG_722t1:c.709C>A	NP_000101.2:p.Pro237Thr
XM_005270562.3:c.709C>A	XP_005270619.2:p.Pro237Thr
XM_006710397.2:c.709C>A	XP_006710460.1:p.Pro237Thr
XM_006710397.3:c.709C>A	XP_006710460.1:p.Pro237Thr
XM_017000507.1:c.598C>A	XP_016855996.1:p.Pro200Thr
XM_017000508.2:c.214C>A	XP_016855997.1:p.Pro72Thr
XM_017000509.2:c.214C>A	XP_016855998.1:p.Pro72Thr
XM_017000510.1:c.214C>A	XP_016855999.1:p.Pro72Thr
NM_000110.4:c.709C>A MANE Select	NP_000101.2:p.Pro237Thr