Canonical Allele Identifier: CA419137410

Gene: DPYD DPYD-AS1

Linked Data

• dbSNP Id: rs2101035595
• MyVariant Identifiers: chr1:g.97770825T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97305269T>C , CM000663.2:g.97305269T>C	GRCh38
NC_000001.10:g.97770825T>C , CM000663.1:g.97770825T>C	GRCh37
NC_000001.9:g.97543413T>C	NCBI36
NG_008807.2:g.620791A>G , LRG_722:g.620791A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.2289A>G (DPYD) MANE Select	ENSP00000359211.3:p.Gly763=
ENST00000370192.7:c.2289A>G (DPYD)	ENSP00000359211.3:p.Gly763=
NM_000110.3:c.2289A>G , LRG_722t1:c.2289A>G (DPYD)	NP_000101.2:p.Gly763=
NR_046590.1:n.129-920T>C (DPYD-AS1)
XM_005270562.3:c.2073A>G (DPYD)	XP_005270619.2:p.Gly691=
XM_006710397.2:c.2289A>G (DPYD)	XP_006710460.1:p.Gly763=
XM_006710397.3:c.2289A>G (DPYD)	XP_006710460.1:p.Gly763=
XM_017000507.1:c.2178A>G (DPYD)	XP_016855996.1:p.Gly726=
XM_017000508.2:c.1794A>G (DPYD)	XP_016855997.1:p.Gly598=
XM_017000509.2:c.1794A>G (DPYD)	XP_016855998.1:p.Gly598=
XM_017000510.1:c.1794A>G (DPYD)	XP_016855999.1:p.Gly598=
NM_000110.4:c.2289A>G (DPYD) MANE Select	NP_000101.2:p.Gly763=