Canonical Allele Identifier: CA419137408

Gene: DPYD DPYD-AS1

Linked Data

• MyVariant Identifiers: chr1:g.97770822T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97305266T>G , CM000663.2:g.97305266T>G	GRCh38
NC_000001.10:g.97770822T>G , CM000663.1:g.97770822T>G	GRCh37
NC_000001.9:g.97543410T>G	NCBI36
NG_008807.2:g.620794A>C , LRG_722:g.620794A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.2292A>C (DPYD) MANE Select	ENSP00000359211.3:p.Gly764=
ENST00000370192.7:c.2292A>C (DPYD)	ENSP00000359211.3:p.Gly764=
NM_000110.3:c.2292A>C , LRG_722t1:c.2292A>C (DPYD)	NP_000101.2:p.Gly764=
NR_046590.1:n.129-923T>G (DPYD-AS1)
XM_005270562.3:c.2076A>C (DPYD)	XP_005270619.2:p.Gly692=
XM_006710397.2:c.2292A>C (DPYD)	XP_006710460.1:p.Gly764=
XM_006710397.3:c.2292A>C (DPYD)	XP_006710460.1:p.Gly764=
XM_017000507.1:c.2181A>C (DPYD)	XP_016855996.1:p.Gly727=
XM_017000508.2:c.1797A>C (DPYD)	XP_016855997.1:p.Gly599=
XM_017000509.2:c.1797A>C (DPYD)	XP_016855998.1:p.Gly599=
XM_017000510.1:c.1797A>C (DPYD)	XP_016855999.1:p.Gly599=
NM_000110.4:c.2292A>C (DPYD) MANE Select	NP_000101.2:p.Gly764=